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misoprostol - 55289-640-04 - (misoprostol)

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Drug Information of misoprostol

Product NDC: 55289-640
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: 55289-640
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019268
Marketing Category: NDA
Start Marketing Date: 20091227

Package Information of misoprostol

Package NDC: 55289-640-04
Package Description: 4 TABLET in 1 BOTTLE, PLASTIC (55289-640-04)

NDC Information of misoprostol

NDC Code 55289-640-04
Proprietary Name misoprostol
Package Description 4 TABLET in 1 BOTTLE, PLASTIC (55289-640-04)
Product NDC 55289-640
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
Labeler Name PD-Rx 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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