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OXYCODONE AND ACETAMINOPHEN - 42549-615-02 - (oxycodone hydrochloride and acetaminophen)

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Drug Information of OXYCODONE AND ACETAMINOPHEN

Product NDC: 42549-615
Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Non Proprietary Name: oxycodone hydrochloride and acetaminophen
Active Ingredient(s): 325; 7.5    mg/1; mg/1 & nbsp;   oxycodone hydrochloride and acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of OXYCODONE AND ACETAMINOPHEN

Product NDC: 42549-615
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040545
Marketing Category: ANDA
Start Marketing Date: 20090401

Package Information of OXYCODONE AND ACETAMINOPHEN

Package NDC: 42549-615-02
Package Description: 112 TABLET in 1 BOTTLE (42549-615-02)

NDC Information of OXYCODONE AND ACETAMINOPHEN

NDC Code 42549-615-02
Proprietary Name OXYCODONE AND ACETAMINOPHEN
Package Description 112 TABLET in 1 BOTTLE (42549-615-02)
Product NDC 42549-615
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090401
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 325; 7.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OXYCODONE AND ACETAMINOPHEN


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