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Clomiphene Citrate - 21695-114-10 - (Clomiphene Citrate)

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Drug Information of Clomiphene Citrate

Product NDC: 21695-114
Proprietary Name: Clomiphene Citrate
Non Proprietary Name: Clomiphene Citrate
Active Ingredient(s): 50    mg/1 & nbsp;   Clomiphene Citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clomiphene Citrate

Product NDC: 21695-114
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075528
Marketing Category: ANDA
Start Marketing Date: 19990830

Package Information of Clomiphene Citrate

Package NDC: 21695-114-10
Package Description: 1 BLISTER PACK in 1 CARTON (21695-114-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Clomiphene Citrate

NDC Code 21695-114-10
Proprietary Name Clomiphene Citrate
Package Description 1 BLISTER PACK in 1 CARTON (21695-114-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 21695-114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clomiphene Citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990830
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CLOMIPHENE CITRATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]

Complete Information of Clomiphene Citrate


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