Cytotec - 55154-3624-0 - (misoprostol)

Alphabetical Index


Drug Information of Cytotec

Product NDC: 55154-3624
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: 55154-3624
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019268
Marketing Category: NDA
Start Marketing Date: 19881227

Package Information of Cytotec

Package NDC: 55154-3624-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-3624-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Cytotec

NDC Code 55154-3624-0
Proprietary Name Cytotec
Package Description 10 BLISTER PACK in 1 BAG (55154-3624-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-3624
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name misoprostol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19881227
Marketing Category Name NDA
Labeler Name Cardinal Health
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