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HYDROCODONE BITARTRATE AND IBUPROFEN - 62037-524-01 - (HYDROCODONE BITARTRATE AND IBUPROFEN)

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Drug Information of HYDROCODONE BITARTRATE AND IBUPROFEN

Product NDC: 62037-524
Proprietary Name: HYDROCODONE BITARTRATE AND IBUPROFEN
Non Proprietary Name: HYDROCODONE BITARTRATE AND IBUPROFEN
Active Ingredient(s): 7.5; 200    mg/1; mg/1 & nbsp;   HYDROCODONE BITARTRATE AND IBUPROFEN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of HYDROCODONE BITARTRATE AND IBUPROFEN

Product NDC: 62037-524
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076604
Marketing Category: ANDA
Start Marketing Date: 20040401

Package Information of HYDROCODONE BITARTRATE AND IBUPROFEN

Package NDC: 62037-524-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62037-524-01)

NDC Information of HYDROCODONE BITARTRATE AND IBUPROFEN

NDC Code 62037-524-01
Proprietary Name HYDROCODONE BITARTRATE AND IBUPROFEN
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62037-524-01)
Product NDC 62037-524
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE AND IBUPROFEN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040401
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name HYDROCODONE BITARTRATE; IBUPROFEN
Strength Number 7.5; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of HYDROCODONE BITARTRATE AND IBUPROFEN


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