Ibuprofen - 49349-613-02 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 49349-613
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 800    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 49349-613
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075682
Marketing Category: ANDA
Start Marketing Date: 20110311

Package Information of Ibuprofen

Package NDC: 49349-613-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-613-02)

NDC Information of Ibuprofen

NDC Code 49349-613-02
Proprietary Name Ibuprofen
Package Description 30 TABLET in 1 BLISTER PACK (49349-613-02)
Product NDC 49349-613
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110311
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name IBUPROFEN
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Ibuprofen


General Information