Prefest is a Kit in the Human Prescription Drug category. It is labeled and distributed by Teva Women's Health, Inc.. The primary component is .
Product ID | 51285-063_35daa1e5-640d-46a6-b25a-bfd1979049e3 |
NDC | 51285-063 |
Product Type | Human Prescription Drug |
Proprietary Name | Prefest |
Generic Name | Estradiol/norgestimate |
Dosage Form | Kit |
Marketing Start Date | 2006-05-30 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA076812 |
Labeler Name | Teva Women's Health, Inc. |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2006-05-30 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA076812 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-08-10 |
Marketing Category | ANDA |
Application Number | ANDA076812 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-05-30 |
SPL SET ID: | 70d00600-b8d3-4820-8db6-40d4536a6f9e |
Manufacturer | |
RxNorm Concept Unique ID - RxCUI |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PREFEST 76412469 2744696 Live/Registered |
TEVA WOMEN'S HEALTH, LLC 2002-05-24 |
PREFEST 75520900 not registered Dead/Abandoned |
JOHNSON & JOHNSON 1998-07-17 |