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Misoprostol - 43063-418-04 - (Misoprostol)

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Drug Information of Misoprostol

Product NDC: 43063-418
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: 43063-418
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091667
Marketing Category: ANDA
Start Marketing Date: 20120725

Package Information of Misoprostol

Package NDC: 43063-418-04
Package Description: 4 TABLET in 1 BOTTLE, PLASTIC (43063-418-04)

NDC Information of Misoprostol

NDC Code 43063-418-04
Proprietary Name Misoprostol
Package Description 4 TABLET in 1 BOTTLE, PLASTIC (43063-418-04)
Product NDC 43063-418
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 PD-Rx Pharmaceuticals, 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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