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Hydrocodone Bitartrate and Acetaminophen - 62037-567-05 - (Hydrocodone Bitartrate and Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 62037-567
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: 62037-567
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040495
Marketing Category: ANDA
Start Marketing Date: 20030528

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 62037-567-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (62037-567-05)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 62037-567-05
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (62037-567-05)
Product NDC 62037-567
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030528
Marketing Category Name ANDA
Labeler Name Watson Pharma, 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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