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MISOPROSTOL - 12634-502-92 - (MISOPROSTOL)

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Drug Information of MISOPROSTOL

Product NDC: 12634-502
Proprietary Name: MISOPROSTOL
Non Proprietary Name: MISOPROSTOL
Active Ingredient(s): 200    ug/1 & nbsp;   MISOPROSTOL
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of MISOPROSTOL

Product NDC: 12634-502
Labeler Name: Apotheca, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019268
Marketing Category: NDA
Start Marketing Date: 19970917

Package Information of MISOPROSTOL

Package NDC: 12634-502-92
Package Description: 2 TABLET in 1 BOTTLE (12634-502-92)

NDC Information of MISOPROSTOL

NDC Code 12634-502-92
Proprietary Name MISOPROSTOL
Package Description 2 TABLET in 1 BOTTLE (12634-502-92)
Product NDC 12634-502
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MISOPROSTOL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970917
Marketing Category Name NDA
Labeler Name Apotheca, Inc.
Substance Name MISOPROSTOL
Strength Number 200
Strength Unit ug/1
Pharmaceutical Classes Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [Chemical/Ingredient]

Complete Information of MISOPROSTOL


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