Cytotec - 54868-2176-4 - (misoprostol)

Alphabetical Index


Drug Information of Cytotec

Product NDC: 54868-2176
Proprietary Name: Cytotec
Non Proprietary Name: misoprostol
Active Ingredient(s): 100    ug/1 & nbsp;   misoprostol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cytotec

Product NDC: 54868-2176
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019268
Marketing Category: NDA
Start Marketing Date: 19960702

Package Information of Cytotec

Package NDC: 54868-2176-4
Package Description: 20 TABLET in 1 BOTTLE (54868-2176-4)

NDC Information of Cytotec

NDC Code 54868-2176-4
Proprietary Name Cytotec
Package Description 20 TABLET in 1 BOTTLE (54868-2176-4)
Product NDC 54868-2176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name misoprostol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960702
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name MISOPROSTOL
Strength Number 100
Strength Unit ug/1
Pharmaceutical Classes Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [Chemical/Ingredient]

Complete Information of Cytotec


General Information