Premarin - 0046-1102-51 - (ESTROGENS, CONJUGATED)

Alphabetical Index


Drug Information of Premarin

Product NDC: 0046-1102
Proprietary Name: Premarin
Non Proprietary Name: ESTROGENS, CONJUGATED
Active Ingredient(s): .625    mg/1 & nbsp;   ESTROGENS, CONJUGATED
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Premarin

Product NDC: 0046-1102
Labeler Name: Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA004782
Marketing Category: NDA
Start Marketing Date: 20060101

Package Information of Premarin

Package NDC: 0046-1102-51
Package Description: 1 POUCH in 1 CARTON (0046-1102-51) > 1 BLISTER PACK in 1 POUCH > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Premarin

NDC Code 0046-1102-51
Proprietary Name Premarin
Package Description 1 POUCH in 1 CARTON (0046-1102-51) > 1 BLISTER PACK in 1 POUCH > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0046-1102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ESTROGENS, CONJUGATED
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060101
Marketing Category Name NDA
Labeler Name Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
Substance Name ESTROGENS, CONJUGATED
Strength Number .625
Strength Unit mg/1
Pharmaceutical Classes Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient]

Complete Information of Premarin


General Information