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Hydrocodone Bitartate and Acetaminophen - 76519-1011-1 - (HYDROCODONE BITARTRATE, ACETAMINOPHEN)

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Drug Information of Hydrocodone Bitartate and Acetaminophen

Product NDC: 76519-1011
Proprietary Name: Hydrocodone Bitartate and Acetaminophen
Non Proprietary Name: HYDROCODONE BITARTRATE, ACETAMINOPHEN
Active Ingredient(s): 325; 2.5    mg/1; mg/1 & nbsp;   HYDROCODONE BITARTRATE, ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartate and Acetaminophen

Product NDC: 76519-1011
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040846
Marketing Category: ANDA
Start Marketing Date: 20120517

Package Information of Hydrocodone Bitartate and Acetaminophen

Package NDC: 76519-1011-1
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC (76519-1011-1)

NDC Information of Hydrocodone Bitartate and Acetaminophen

NDC Code 76519-1011-1
Proprietary Name Hydrocodone Bitartate and Acetaminophen
Package Description 12 TABLET in 1 BOTTLE, PLASTIC (76519-1011-1)
Product NDC 76519-1011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE, ACETAMINOPHEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120517
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 325; 2.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Hydrocodone Bitartate and Acetaminophen


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