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Misoprostol - 40032-161-06 - (Misoprostol)

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Drug Information of Misoprostol

Product NDC: 40032-161
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: 40032-161
Labeler Name: Novel Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091667
Marketing Category: ANDA
Start Marketing Date: 20120725

Package Information of Misoprostol

Package NDC: 40032-161-06
Package Description: 60 TABLET in 1 BOTTLE (40032-161-06)

NDC Information of Misoprostol

NDC Code 40032-161-06
Proprietary Name Misoprostol
Package Description 60 TABLET in 1 BOTTLE (40032-161-06)
Product NDC 40032-161
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Misoprostol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120725
Marketing Category Name ANDA
Labeler Name Novel Laboratories, 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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