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Hydrocodone Bitartrate and Acetaminophen - 64376-640-16 - (Hydrocodone Bitartrate, Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 64376-640
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate, Acetaminophen
Active Ingredient(s): 325; 7.5    mg/15mL; mg/15mL & nbsp;   Hydrocodone Bitartrate, Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 64376-640
Labeler Name: Boca Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040894
Marketing Category: ANDA
Start Marketing Date: 20110727

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 64376-640-16
Package Description: 473 mL in 1 BOTTLE (64376-640-16)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 64376-640-16
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 473 mL in 1 BOTTLE (64376-640-16)
Product NDC 64376-640
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate, Acetaminophen
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110727
Marketing Category Name ANDA
Labeler Name Boca Pharmacal, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 325; 7.5
Strength Unit mg/15mL; mg/15mL
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Hydrocodone Bitartrate and Acetaminophen


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