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HYDROCODONE BITARTRATE AND IBUPROFEN - 54868-4976-6 - (HYDROCODONE BITARTRATE AND IBUPROFEN)

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Drug Information of HYDROCODONE BITARTRATE AND IBUPROFEN

Product NDC: 54868-4976
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: 54868-4976
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076604
Marketing Category: ANDA
Start Marketing Date: 20050725

Package Information of HYDROCODONE BITARTRATE AND IBUPROFEN

Package NDC: 54868-4976-6
Package Description: 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-6)

NDC Information of HYDROCODONE BITARTRATE AND IBUPROFEN

NDC Code 54868-4976-6
Proprietary Name HYDROCODONE BITARTRATE AND IBUPROFEN
Package Description 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4976-6)
Product NDC 54868-4976
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 20050725
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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