Premarin - 54868-0453-0 - (conjugated estrogens)

Alphabetical Index


Drug Information of Premarin

Product NDC: 54868-0453
Proprietary Name: Premarin
Non Proprietary Name: conjugated estrogens
Active Ingredient(s): 1.25    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: 54868-0453
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA004782
Marketing Category: NDA
Start Marketing Date: 20050624

Package Information of Premarin

Package NDC: 54868-0453-0
Package Description: 25 TABLET, FILM COATED in 1 BOTTLE (54868-0453-0)

NDC Information of Premarin

NDC Code 54868-0453-0
Proprietary Name Premarin
Package Description 25 TABLET, FILM COATED in 1 BOTTLE (54868-0453-0)
Product NDC 54868-0453
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name conjugated estrogens
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050624
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ESTROGENS, CONJUGATED
Strength Number 1.25
Strength Unit mg/1
Pharmaceutical Classes Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient]

Complete Information of Premarin


General Information