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MISOPROSTOL - 12634-980-84 - (MISOPROSTOL)

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Drug Information of MISOPROSTOL

Product NDC: 12634-980
Proprietary Name: MISOPROSTOL
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 MISOPROSTOL

Product NDC: 12634-980
Labeler Name: Apotheca, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076095
Marketing Category: ANDA
Start Marketing Date: 20100225

Package Information of MISOPROSTOL

Package NDC: 12634-980-84
Package Description: 14 TABLET in 1 BOTTLE (12634-980-84)

NDC Information of MISOPROSTOL

NDC Code 12634-980-84
Proprietary Name MISOPROSTOL
Package Description 14 TABLET in 1 BOTTLE (12634-980-84)
Product NDC 12634-980
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MISOPROSTOL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100225
Marketing Category Name ANDA
Labeler Name Apotheca, 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 MISOPROSTOL


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