Prometrium - 54868-4230-2 - (progesterone)

Alphabetical Index


Drug Information of Prometrium

Product NDC: 54868-4230
Proprietary Name: Prometrium
Non Proprietary Name: progesterone
Active Ingredient(s): 200    mg/1 & nbsp;   progesterone
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Prometrium

Product NDC: 54868-4230
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019781
Marketing Category: NDA
Start Marketing Date: 20041103

Package Information of Prometrium

Package NDC: 54868-4230-2
Package Description: 5 CAPSULE in 1 BOTTLE (54868-4230-2)

NDC Information of Prometrium

NDC Code 54868-4230-2
Proprietary Name Prometrium
Package Description 5 CAPSULE in 1 BOTTLE (54868-4230-2)
Product NDC 54868-4230
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name progesterone
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20041103
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name PROGESTERONE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Progesterone [Chemical/Ingredient],Progesterone [EPC]

Complete Information of Prometrium


General Information