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Hydrocodone Bitartate and Acetaminophen - 63629-4731-5 - (HYDROCODONE BITARTRATE, ACETAMINOPHEN)

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Drug Information of Hydrocodone Bitartate and Acetaminophen

Product NDC: 63629-4731
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: 63629-4731
Labeler Name: Bryant Ranch Prepack
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: 63629-4731-5
Package Description: 100 TABLET in 1 BOTTLE (63629-4731-5)

NDC Information of Hydrocodone Bitartate and Acetaminophen

NDC Code 63629-4731-5
Proprietary Name Hydrocodone Bitartate and Acetaminophen
Package Description 100 TABLET in 1 BOTTLE (63629-4731-5)
Product NDC 63629-4731
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 Bryant Ranch Prepack
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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