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clomiphene citrate - 43063-250-05 - (clomiphene citrate)

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Drug Information of clomiphene citrate

Product NDC: 43063-250
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: 43063-250
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016131
Marketing Category: NDA
Start Marketing Date: 19670201

Package Information of clomiphene citrate

Package NDC: 43063-250-05
Package Description: 5 TABLET in 1 BOTTLE, PLASTIC (43063-250-05)

NDC Information of clomiphene citrate

NDC Code 43063-250-05
Proprietary Name clomiphene citrate
Package Description 5 TABLET in 1 BOTTLE, PLASTIC (43063-250-05)
Product NDC 43063-250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clomiphene citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19670201
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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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