NDC 51285-063
Prefest
Estradiol/norgestimate
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 |
Packaging
NDC 51285-063-90
6 POUCH in 1 CARTON (51285-063-90) > 1 BLISTER PACK in 1 POUCH (51285-063-89) > 1 KIT in 1 BLISTER PACK
| Marketing Start Date | 2006-05-30 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 51285-063-89 [51285006389]
Prefest KIT
| Marketing Category | ANDA |
| Application Number | ANDA076812 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-08-10 |
NDC 51285-063-90 [51285006390]
Prefest KIT
| Marketing Category | ANDA |
| Application Number | ANDA076812 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2006-05-30 |
Drug Details
OpenFDA Data
| SPL SET ID: | 70d00600-b8d3-4820-8db6-40d4536a6f9e |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |
Medicade Reported Pricing
51285006390 PREFEST TABLET
Pricing Unit: EA | Drug Type:
Trademark Results [Prefest]
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 |
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