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Hydrocodone Bitartrate and Acetaminophen - 17856-1295-1 - (Hydrocodone Bitartrate and Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 17856-1295
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Active Ingredient(s): 500; 7.5    mg/15mL; mg/15mL & nbsp;   Hydrocodone Bitartrate and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 17856-1295
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040520
Marketing Category: ANDA
Start Marketing Date: 20031030

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 17856-1295-1
Package Description: 15 mL in 1 CUP (17856-1295-1)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 17856-1295-1
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 15 mL in 1 CUP (17856-1295-1)
Product NDC 17856-1295
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20031030
Marketing Category Name ANDA
Labeler Name Atlantic Biologicals Corps
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 500; 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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