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Premarin
Premarin - 0046-0749-05 - (conjugated estrogens)
Drug Information of Premarin
| Product NDC: | 0046-0749 |
| Proprietary Name: | Premarin |
| Non Proprietary Name: | conjugated estrogens |
| Active Ingredient(s): | 25 mg/5mL & nbsp; conjugated estrogens |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Premarin
| Product NDC: | 0046-0749 |
| Labeler Name: | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA010402 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19561201 |
Package Information of Premarin
| Package NDC: | 0046-0749-05 |
| Package Description: | 1 VIAL in 1 CARTON (0046-0749-05) > 25 mL in 1 VIAL |
NDC Information of Premarin
| NDC Code | 0046-0749-05 |
| Proprietary Name | Premarin |
| Package Description | 1 VIAL in 1 CARTON (0046-0749-05) > 25 mL in 1 VIAL |
| Product NDC | 0046-0749 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | conjugated estrogens |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19561201 |
| Marketing Category Name | NDA |
| Labeler Name | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
| Substance Name | ESTROGENS, CONJUGATED |
| Strength Number | 25 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient] |
