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Hydrocodone Bitartrate and Acetaminophen - 63304-497-11 - (Hydrocodone Bitartrate and Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 63304-497
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: 63304-497
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040826
Marketing Category: ANDA
Start Marketing Date: 20080815

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 63304-497-11
Package Description: 10 TABLET in 1 BLISTER PACK (63304-497-11)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 63304-497-11
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 10 TABLET in 1 BLISTER PACK (63304-497-11)
Product NDC 63304-497
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080815
Marketing Category Name ANDA
Labeler Name Ranbaxy Pharmaceuticals 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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