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ClomiPHENE Citrate
ClomiPHENE Citrate - 0093-0041-65 - (ClomiPHENE citrate)
Drug Information of ClomiPHENE Citrate
| Product NDC: | 0093-0041 |
| 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: | 0093-0041 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018361 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19921101 |
Package Information of ClomiPHENE Citrate
| Package NDC: | 0093-0041-65 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (0093-0041-65) > 10 TABLET in 1 BLISTER PACK |
NDC Information of ClomiPHENE Citrate
| NDC Code | 0093-0041-65 |
| Proprietary Name | ClomiPHENE Citrate |
| Package Description | 3 BLISTER PACK in 1 CARTON (0093-0041-65) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 0093-0041 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ClomiPHENE citrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19921101 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | CLOMIPHENE CITRATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA] |
