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Hydrocodone Bitartrate and Acetaminophen - 0591-0517-01 - (Hydrocodone Bitartrate and Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 0591-0517
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Active Ingredient(s): 660; 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: 0591-0517
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040094
Marketing Category: ANDA
Start Marketing Date: 20000808

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 0591-0517-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0591-0517-01)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 0591-0517-01
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0591-0517-01)
Product NDC 0591-0517
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000808
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 660; 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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