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Hydrocodone Bitartrate and Acetaminophen - 24236-359-08 - (HYDROCODONE BITARTRATE)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 24236-359
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: HYDROCODONE BITARTRATE
Active Ingredient(s): 325; 10    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: 24236-359
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040355
Marketing Category: ANDA
Start Marketing Date: 20121224

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 24236-359-08
Package Description: 10 TABLET in 1 VIAL (24236-359-08)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 24236-359-08
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 10 TABLET in 1 VIAL (24236-359-08)
Product NDC 24236-359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121224
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 325; 10
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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