Product NDC: | 54868-3059 |
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) |
Product NDC: | 54868-3059 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075528 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960822 |
Package NDC: | 54868-3059-1 |
Package Description: | 1 BLISTER PACK in 1 BOTTLE, DISPENSING (54868-3059-1) > 10 TABLET in 1 BLISTER PACK |
NDC Code | 54868-3059-1 |
Proprietary Name | Clomiphene Citrate |
Package Description | 1 BLISTER PACK in 1 BOTTLE, DISPENSING (54868-3059-1) > 10 TABLET in 1 BLISTER PACK |
Product NDC | 54868-3059 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clomiphene Citrate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19960822 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | CLOMIPHENE CITRATE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA] |