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Hydrocodone Bitartrate and Acetaminophen - 24236-068-07 - (HYDROCODONE BITARTRATE)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 24236-068
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: HYDROCODONE BITARTRATE
Active Ingredient(s): 500; 5    mg/1; mg/1 & nbsp;   HYDROCODONE BITARTRATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 24236-068
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040084
Marketing Category: ANDA
Start Marketing Date: 20120910

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 24236-068-07
Package Description: 12 TABLET in 1 BLISTER PACK (24236-068-07)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 24236-068-07
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 12 TABLET in 1 BLISTER PACK (24236-068-07)
Product NDC 24236-068
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120910
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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