NDC 63629-2165

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 ID63629-2165_6370e342-16a5-4339-a13f-ba275fd5de09
NDC63629-2165
Product TypeHuman Prescription Drug
Proprietary NameClomiphene Citrate
Generic NameClomiphene Citrate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1999-08-30
Marketing CategoryANDA /
Application NumberANDA075528
Labeler NameBryant Ranch Prepack
Substance NameCLOMIPHENE CITRATE
Active Ingredient Strength50 mg/1
Pharm ClassesEstrogen Agonist/Antagonist [EPC], Selective Estrogen Receptor Modulators [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63629-2165-1

30 TABLET in 1 BLISTER PACK (63629-2165-1)
Marketing Start Date2022-02-08
NDC Exclude FlagN
Sample Package?N

Drug Details

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

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.