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Hydrocodone Bitartrate and Acetaminophen - 63629-4272-6 - (Hydrocodone Bitartrate and Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 63629-4272
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Active Ingredient(s): 325; 10    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: 63629-4272
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040148
Marketing Category: ANDA
Start Marketing Date: 20130307

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 63629-4272-6
Package Description: 140 TABLET in 1 BOTTLE (63629-4272-6)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 63629-4272-6
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 140 TABLET in 1 BOTTLE (63629-4272-6)
Product NDC 63629-4272
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130307
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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