NDC 63629-5302

Clomiphene Citrate

Clomiphene Citrate

Clomiphene Citrate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Clomiphene Citrate.

Product ID63629-5302_7ac50bfe-7054-4174-b418-61bacab5a77b
NDC63629-5302
Product TypeHuman Prescription Drug
Proprietary NameClomiphene Citrate
Generic NameClomiphene Citrate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1999-08-30
Marketing CategoryANDA / ANDA
Application NumberANDA075528
Labeler NameBryant Ranch Prepack
Substance NameCLOMIPHENE CITRATE
Active Ingredient Strength50 mg/1
Pharm ClassesSelective Estrogen Receptor Modulators [MoA],Estrogen Agonist/Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 63629-5302-1

30 TABLET in 1 BOTTLE (63629-5302-1)
Marketing Start Date2020-04-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-5302-3 [63629530203]

Clomiphene Citrate TABLET
Marketing CategoryANDA
Application NumberANDA075528
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-01

NDC 63629-5302-4 [63629530204]

Clomiphene Citrate TABLET
Marketing CategoryANDA
Application NumberANDA075528
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-01

NDC 63629-5302-1 [63629530201]

Clomiphene Citrate TABLET
Marketing CategoryANDA
Application NumberANDA075528
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-01

NDC 63629-5302-5 [63629530205]

Clomiphene Citrate TABLET
Marketing CategoryANDA
Application NumberANDA075528
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-01

NDC 63629-5302-6 [63629530206]

Clomiphene Citrate TABLET
Marketing CategoryANDA
Application NumberANDA075528
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-01

NDC 63629-5302-2 [63629530202]

Clomiphene Citrate TABLET
Marketing CategoryANDA
Application NumberANDA075528
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-03-01

Drug Details

Active Ingredients

IngredientStrength
CLOMIPHENE CITRATE50 mg/1

OpenFDA Data

SPL SET ID:d1c19ed9-fdee-4c65-a4bf-58d5f33638ec
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1093060

    • Pharmacological Class

    • Selective Estrogen Receptor Modulators [MoA]
    • Estrogen Agonist/Antagonist [EPC]

    NDC Crossover Matching brand name "Clomiphene Citrate" or generic name "Clomiphene Citrate"

    NDCBrand NameGeneric Name
    21695-114Clomiphene CitrateClomiphene Citrate
    49884-701Clomiphene CitrateClomiphene Citrate
    50090-0677Clomiphene CitrateClomiphene Citrate
    50090-0678Clomiphene CitrateClomiphene Citrate
    61919-375CLOMIPHENE CITRATECLOMIPHENE CITRATE
    63629-2165Clomiphene CitrateClomiphene Citrate
    63629-5302Clomiphene CitrateClomiphene Citrate
    63629-9276Clomiphene CitrateClomiphene Citrate
    68071-2166Clomiphene CitrateClomiphene Citrate
    68071-2638Clomiphene CitrateClomiphene Citrate
    68071-4676Clomiphene CitrateClomiphene Citrate
    0713-0885ClomidClomiphene Citrate
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