ibuprofen - 49614-116-78 - (Ibuprofen)

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Drug Information of ibuprofen

Product NDC: 49614-116
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 49614-116
Labeler Name: Medicine Shoppe International Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 19880315

Package Information of ibuprofen

Package NDC: 49614-116-78
Package Description: 1 BOTTLE in 1 CARTON (49614-116-78) > 100 TABLET, FILM COATED in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 49614-116-78
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (49614-116-78) > 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC 49614-116
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19880315
Marketing Category Name ANDA
Labeler Name Medicine Shoppe International Inc
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ibuprofen


General Information