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HYDROCODONE BITARTRATE AND ACETAMINOPHEN - 67296-0470-4 - (hydrocodone bitartrate and acetaminophen)

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Drug Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product NDC: 67296-0470
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: 67296-0470
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089971
Marketing Category: ANDA
Start Marketing Date: 19981202

Package Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Package NDC: 67296-0470-4
Package Description: 14 TABLET in 1 BOTTLE (67296-0470-4)

NDC Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

NDC Code 67296-0470-4
Proprietary Name HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Package Description 14 TABLET in 1 BOTTLE (67296-0470-4)
Product NDC 67296-0470
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocodone bitartrate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19981202
Marketing Category Name ANDA
Labeler Name RedPharm Drug Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 500; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

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