Cytotec - 55289-248-28 - (misoprostol)

Alphabetical Index


Drug Information of Cytotec

Product NDC: 55289-248
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: 55289-248
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019268
Marketing Category: NDA
Start Marketing Date: 19861227

Package Information of Cytotec

Package NDC: 55289-248-28
Package Description: 28 TABLET in 1 BOTTLE, PLASTIC (55289-248-28)

NDC Information of Cytotec

NDC Code 55289-248-28
Proprietary Name Cytotec
Package Description 28 TABLET in 1 BOTTLE, PLASTIC (55289-248-28)
Product NDC 55289-248
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name misoprostol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19861227
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, 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