Premarin - 55154-0216-0 - (conjugated estrogens)

Alphabetical Index


Drug Information of Premarin

Product NDC: 55154-0216
Proprietary Name: Premarin
Non Proprietary Name: conjugated estrogens
Active Ingredient(s): .625    mg/1 & nbsp;   conjugated estrogens
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Premarin

Product NDC: 55154-0216
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA004782
Marketing Category: NDA
Start Marketing Date: 20060101

Package Information of Premarin

Package NDC: 55154-0216-0
Package Description: 10 POUCH in 1 BAG (55154-0216-0) > 1 TABLET, FILM COATED in 1 POUCH

NDC Information of Premarin

NDC Code 55154-0216-0
Proprietary Name Premarin
Package Description 10 POUCH in 1 BAG (55154-0216-0) > 1 TABLET, FILM COATED in 1 POUCH
Product NDC 55154-0216
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name conjugated estrogens
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060101
Marketing Category Name NDA
Labeler Name Cardinal Health
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