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 ID51285-063_35daa1e5-640d-46a6-b25a-bfd1979049e3
NDC51285-063
Product TypeHuman Prescription Drug
Proprietary NamePrefest
Generic NameEstradiol/norgestimate
Dosage FormKit
Marketing Start Date2006-05-30
Marketing CategoryANDA / ANDA
Application NumberANDA076812
Labeler NameTeva Women's Health, Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2022-12-31

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 Date2006-05-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51285-063-89 [51285006389]

Prefest KIT
Marketing CategoryANDA
Application NumberANDA076812
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-08-10

NDC 51285-063-90 [51285006390]

Prefest KIT
Marketing CategoryANDA
Application NumberANDA076812
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-05-30

Drug Details

OpenFDA Data

SPL SET ID:70d00600-b8d3-4820-8db6-40d4536a6f9e
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 197658
  • 749850
  • 348906
  • 762394
  • Medicade Reported Pricing

    51285006390 PREFEST TABLET

    Pricing Unit: EA | Drug Type:

    Trademark Results [Prefest]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PREFEST
    PREFEST
    76412469 2744696 Live/Registered
    TEVA WOMEN'S HEALTH, LLC
    2002-05-24
    PREFEST
    PREFEST
    75520900 not registered Dead/Abandoned
    JOHNSON & JOHNSON
    1998-07-17

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