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Pain Relief Anti inflammatory - 52904-486-02 - (IBUPROFEN)

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Drug Information of Pain Relief Anti inflammatory

Product NDC: 52904-486
Proprietary Name: Pain Relief Anti inflammatory
Non Proprietary Name: IBUPROFEN
Active Ingredient(s): 200    mg/1 & nbsp;   IBUPROFEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pain Relief Anti inflammatory

Product NDC: 52904-486
Labeler Name: Select Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091239
Marketing Category: ANDA
Start Marketing Date: 20121015

Package Information of Pain Relief Anti inflammatory

Package NDC: 52904-486-02
Package Description: 2 TABLET in 1 PACKET (52904-486-02)

NDC Information of Pain Relief Anti inflammatory

NDC Code 52904-486-02
Proprietary Name Pain Relief Anti inflammatory
Package Description 2 TABLET in 1 PACKET (52904-486-02)
Product NDC 52904-486
Product Type Name HUMAN OTC DRUG
Non Proprietary Name IBUPROFEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121015
Marketing Category Name ANDA
Labeler Name Select Corporation
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Pain Relief Anti inflammatory


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