Premarin - 0046-0872-08 - (conjugated estrogens)

Alphabetical Index


Drug Information of Premarin

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)

Labeler Information of Premarin

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 Information of Premarin

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 Information of Premarin

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]

Complete Information of Premarin


General Information