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Misoprostol - 0172-4430-59 - (Misoprostol)

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Drug Information of Misoprostol

Product NDC: 0172-4430
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: 0172-4430
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076095
Marketing Category: ANDA
Start Marketing Date: 20020710

Package Information of Misoprostol

Package NDC: 0172-4430-59
Package Description: 120 TABLET in 1 BOTTLE, UNIT-DOSE (0172-4430-59)

NDC Information of Misoprostol

NDC Code 0172-4430-59
Proprietary Name Misoprostol
Package Description 120 TABLET in 1 BOTTLE, UNIT-DOSE (0172-4430-59)
Product NDC 0172-4430
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Misoprostol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020710
Marketing Category Name ANDA
Labeler Name IVAX 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 Misoprostol


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