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Updated: 10/2/2017
Table of Contents
Therapeutic Equivalence Ratings 1
Latex Content 1
Generic Products 2
Brand-to-Generic Index 18
With Teva's recent acquisition of Actavis Generics, we provide an even stronger commitment to
innovation, quality, and improving people's health around the world. We are pleased to present this
combined catalog of all Teva and Actavis products.
While we work to fully integrate our two systems, please use the following customer service contact
information for ordering and questions relating to each company's product. Actavis products are
indicated with an .
Drug products the FDA considers therapeutically equivalent to other pharmaceutically equivalent products. These codes are
published in FDA’s Orange Book:
AA Products in conventional dosage forms not presenting bioequivalence problems
AB Products meeting necessary bioequivalence requirements
AB1 Products meeting necessary bioequivalence requirements, assigned when more than one reference listed drug of the same
strength has been designated under the same heading
AB2 Products meeting necessary bioequivalence requirements, assigned when more than one reference listed drug of the same
strength has been designated under the same heading
AB3 Products meeting necessary bioequivalence requirements, assigned when more than one reference listed drug of the same
strength has been designated under the same heading
AB4 Products meeting necessary bioequivalence requirements, assigned when more than one reference listed drug of the same
strength has been designated under the same heading
AN Solutions and powders for aerosolization
AO Injectable oil solutions
AP Injectable aqueous solutions and, in certain instances, intravenous non-aqueous solutions
AT Topical products
BD Products containing active ingredients with known bioequivalence problems and for which adequate studies have not been
submitted to FDA demonstrating bioequivalence
Latex Content
The term “natural rubber” includes all materials made from or containing natural latex. Products containing natural rubber are made using
two commonly employed manufacturing processes: the natural rubber latex (NRL) process, and the dry natural rubber (DNR) process.
“Natural latex” is defined as a milky fluid that consists of extremely small particles of rubber obtained from plants, principally from the H.
brasiliensis (rubber) tree, dispersed in an aqueous medium. It contains a variety of naturally occurring substances including cis-1,4-
polyisoprene in a colloidal suspension and plant proteins, which are believed to be the primary allergen.
The NRL manufacturing process involves the use of natural latex in a concentrated colloidal suspension. Products are formed from natural
rubber latex by dipping, extruding, or coating, and are typically referred to as containing or made of “natural rubber latex.”
The DNR manufacturing process involves the use of coagulated natural latex in the form of dried or milled sheets. Products are formed
from dry natural rubber by compression molding, extrusion, or by converting the sheets into a solution for dipping. These products are
typically referred to as containing or made of dry natural rubber or “crepe” rubber. Examples of products that may contain dry natural
rubber include syringe plungers, vial stoppers and injection ports on intra-vascular tubing.
For more information from the FDA about natural rubber, please visit www.fda.gov/RegulatoryInformation/Guidances/ucm070925.htm.
Based on the information provided by our suppliers, the product listing in this brochure will relate to a specific component of the medical
product, its container, or any packaging.
Should you have additional questions, please feel free to contact Teva at 888.838.2872.
The icons below are used throughout the product sections to identify key product attributes.
Indicates products that are preservative free, minimizing the risk of side effects and allergic reactions.
Identifies unit dose products and injectable products labeled with a scannable standard code 128 bar code or a
scannable standard RSS bar code. Each bar code contains the NDC number for a single tablet, capsule, or a single vial.
This feature helps ensure accuracy and patient safety when dispensing, and facilitates order entry and inventory
maintenance.
1
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Anastrozole Tablets
AB Rated and bioequivalent to Arimidex® Tablets
1 mg Round, White to Off-White/TEVA/A10 30 00093-7536-56 1 mg
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Carboplatin Injection
AP Rated
10 mg/mL, 50 mg Multiple-Dose Amber Vial 5 mL/Vial 00703-4244-01
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Cisplatin Injection
AP Rated to Platinol®-AQ Injection
1 mg/mL, 50 mg Multiple-Dose Amber Vial 50 mL/Vial 00703-5747-11
The rubber stopper, label material, and adhesive/inks used for the labels are not made with
natural rubber latex. Store at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F).
Retain in the original package to protect from light.
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
* †The vial stopper is made with natural rubber latex. Store refrigerated at 2° to 8°C (36° to 46°F).
Protect from light and retain in carton until time of use.
††The rubber stopper, label material, and adhesive/inks used for the labels are not made with
natural rubber latex. Store under refrigeration between 2° to 8°C (36° to 46°F).Protect from
light. Retain in carton until time of use. Discard unused portion.
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
The container closure is not made of natural rubber latex. Store refrigerated at 2° to 8°C (36° to
46°F). Protect from light and freezing.
The container closure is not made with natural rubber latex. Store at 20°C to 25°C (68°F to 77°F);
excursions permitted between 15°C to 30°C (59°F to 86°F), in the original package.
The vial stopper is not made with natural rubber latex. Store under refrigeration, between 2°
and 8°C (36° to 46°F).
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
The container closure is not made with natural rubber latex. Store at 20° to 25°C (68° to 77°F);
excursions between 15° and 30°C (59° and 86°F).
The container closure is not made with natural rubber latex. Store at 20° to 25°C (68° to 77°F);
excursions between 15° and 30°C (59° and 86°F).
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Gemcitabine Injection
AP Rated
38 mg/mL, 200 mg Single-Use Vial 5.26 mL/Vial 45963-0623-57
The vial stopper is not made with natural rubber latex. Store refrigerated between 2°C to 8°C
(36°F to 46°F)
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Ifosfamide Injection
AP Rated to Ifex® Injection
50 mg/mL, 1 gm Single-Use Vial 20 mL/Vial 00703-3427-11
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
* †The vial and vial stopper are not made with natural rubber latex. Store at 20° to 25°C (68° to
77°F). Protect from light. Do not freeze. Keep in carton until use.
††The container closure is not made with natural rubber latex. Store at 20°C to 25°C (68°F to
77°F) . Protect from light. It is recommended that the vial should remain in the carton until the
time of use.
10
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
The vial stopper is not made with natural rubber latex. Store at 25°C (77°F). Excursions
permitted from 15° to 30°C (59° to 86°F). Protect from light.
The vial stopper is not made with natural rubber latex. Store at 25°C (77°F); excursions
permitted from 15° to 30°C (59° to 86°F). Protect from light.
11
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Mesna Injection
AP Rated to Mesnex® Injection
100 mg/mL, 1 g Multiple-Dose Vial 10 mL/Vial 00703-4805-01
The vial stoppers are not made with natural rubber latex. Store at 2° to 30°C (36° to 86°F).
12
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
The container closure is not made with natural rubber latex. Store at 20° to 25°C (68° to 77°F);
excursions permitted between 15° and 30°C (59° and 86°F). Retain in carton until time of use.
13
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Oxaliplatin Injection
AP Rated
5 mg/mL, 50 mg Single-Use Vial 10 mL/Vial 00703-3985-01
Paclitaxel Injection
AP Rated to Taxol® Injection
6 mg/mL, 30 mg Multiple-Dose Vial 5 mL/Vial 00703-4764-01
The container closure is not made with natural rubber latex. Store at 20° to 25°C (68° to 77°F).
Protect from light. Retain in carton until use.
14
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Temozolomide Capsules
AB Rated and bioequivalent to Temodar® Capsules
5 mg Off-White Opaque/barr 5 mg/1078 5 00093-7599-57 5 mg 20 mg
15
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
The vial stopper and label are not made with natural rubber latex. Store at 20° to 25°C (68° to
77°F). Protect from light.
Topotecan Injection
AP Rated
1 mg/mL, 4 mg Single-Use Vial 4 mL/Vial 00703-4714-01
The vial and vial stopper are not made with natural rubber latex. Store refrigerated at 2° to 8°C
(36° to 46°F). Retain in carton until use.
Tretinoin Capsules
AB Rated and bioequivalent to Vesanoid® Capsules
10 mg Brown Opaque/Dark Yellow Opaque/barr 100 00555-0808-02 10 mg
808
16
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
GENERIC
Strength Description/Imprint Code Size NDC Number
PRODUCTS
Vinorelbine Injection
AP Rated to Navelbine® Injection
1 mg/1 mL, 10mg Single-Use Vial 1 mL/Vial 45963-0607-55
The vial stopper and container closure system is not made with natural rubber latex. Store
refrigerated between 2°C to 8°C (36°F to 46°F). Protect from light.
17
Products not shown actual size. Colors may vary slightly. All trademarks (TM) and registered trademarks (®) are property of their respective companies.
BRAND-TO-GENERIC
INDEX
ACTIQ® oral transmucosal lozenge [C-II] Oral Transmucosal Fentanyl Citrate (OTFC) Lozenges CII 13
18
All trademarks (TM) and registered trandmarks (®) are property of their respective companies.
BRAND-TO-GENERIC
INDEX
Carboplatin Injection 3
Gemcitabine Injection 8
Oxaliplatin Injection 14
Topotecan Injection 16
19
All trademarks (TM) and registered trandmarks (®) are property of their respective companies.