Product NDC: | 0046-0872 |
Proprietary Name: | Premarin |
Non Proprietary Name: | conjugated estrogens |
Active Ingredient(s): | .625 mg/g & nbsp; conjugated estrogens |
Administration Route(s): | VAGINAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0046-0872 |
Labeler Name: | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020216 |
Marketing Category: | NDA |
Start Marketing Date: | 19781101 |
Package NDC: | 0046-0872-08 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (0046-0872-08) > 8 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 0046-0872-08 |
Proprietary Name | Premarin |
Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (0046-0872-08) > 8 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 0046-0872 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | conjugated estrogens |
Dosage Form Name | CREAM |
Route Name | VAGINAL |
Start Marketing Date | 19781101 |
Marketing Category Name | NDA |
Labeler Name | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
Substance Name | ESTROGENS, CONJUGATED |
Strength Number | .625 |
Strength Unit | mg/g |
Pharmaceutical Classes | Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient] |