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smart sense ibuprofen - 49738-461-62 - (Ibuprofen)

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Drug Information of smart sense ibuprofen

Product NDC: 49738-461
Proprietary Name: smart sense ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of smart sense ibuprofen

Product NDC: 49738-461
Labeler Name: Kmart Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076359
Marketing Category: ANDA
Start Marketing Date: 20100624

Package Information of smart sense ibuprofen

Package NDC: 49738-461-62
Package Description: 1 BOTTLE in 1 CARTON (49738-461-62) > 24 TABLET, CHEWABLE in 1 BOTTLE

NDC Information of smart sense ibuprofen

NDC Code 49738-461-62
Proprietary Name smart sense ibuprofen
Package Description 1 BOTTLE in 1 CARTON (49738-461-62) > 24 TABLET, CHEWABLE in 1 BOTTLE
Product NDC 49738-461
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20100624
Marketing Category Name ANDA
Labeler Name Kmart Corporation
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of smart sense ibuprofen


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