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misoprostol - 59762-5007-1 - (MISOPROSTOL)

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Drug Information of misoprostol

Product NDC: 59762-5007
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: 59762-5007
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019268
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20091227

Package Information of misoprostol

Package NDC: 59762-5007-1
Package Description: 60 TABLET in 1 BOTTLE (59762-5007-1)

NDC Information of misoprostol

NDC Code 59762-5007-1
Proprietary Name misoprostol
Package Description 60 TABLET in 1 BOTTLE (59762-5007-1)
Product NDC 59762-5007
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MISOPROSTOL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091227
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
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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