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HYDROCODONE BITARTRATE AND ACETAMINOPHEN - 0339-4146-06 - (HYDROCODONE BITARTRATE AND ACETAMINOPHEN)

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Drug Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product NDC: 0339-4146
Proprietary Name: HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Non Proprietary Name: HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Active Ingredient(s): 500; 5    mg/1; mg/1 & nbsp;   HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product NDC: 0339-4146
Labeler Name: Caremark L.L.C.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089160
Marketing Category: ANDA
Start Marketing Date: 20040505

Package Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Package NDC: 0339-4146-06
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0339-4146-06)

NDC Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

NDC Code 0339-4146-06
Proprietary Name HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0339-4146-06)
Product NDC 0339-4146
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040505
Marketing Category Name ANDA
Labeler Name Caremark L.L.C.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 500; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN


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