Product NDC: | 44087-8090 |
Proprietary Name: | Serophene |
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: | 44087-8090 |
Labeler Name: | EMD Serono, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018361 |
Marketing Category: | NDA |
Start Marketing Date: | 19820322 |
Package NDC: | 44087-8090-6 |
Package Description: | 1 BLISTER PACK in 1 CARTON (44087-8090-6) > 10 TABLET in 1 BLISTER PACK |
NDC Code | 44087-8090-6 |
Proprietary Name | Serophene |
Package Description | 1 BLISTER PACK in 1 CARTON (44087-8090-6) > 10 TABLET in 1 BLISTER PACK |
Product NDC | 44087-8090 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clomiPHENE citrate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19820322 |
Marketing Category Name | NDA |
Labeler Name | EMD Serono, Inc. |
Substance Name | CLOMIPHENE CITRATE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA] |