Prometrium - 0032-1711-01 - (Progesterone)

Alphabetical Index


Drug Information of Prometrium

Product NDC: 0032-1711
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: 0032-1711
Labeler Name: Abbott Products, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019781
Marketing Category: NDA
Start Marketing Date: 20100730

Package Information of Prometrium

Package NDC: 0032-1711-01
Package Description: 100 CAPSULE in 1 BOTTLE (0032-1711-01)

NDC Information of Prometrium

NDC Code 0032-1711-01
Proprietary Name Prometrium
Package Description 100 CAPSULE in 1 BOTTLE (0032-1711-01)
Product NDC 0032-1711
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Progesterone
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100730
Marketing Category Name NDA
Labeler Name Abbott Products, Inc.
Substance Name PROGESTERONE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Progesterone [Chemical/Ingredient],Progesterone [EPC]

Complete Information of Prometrium


General Information