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Oxycodone Hydrochloride and Acetaminophen - 42549-618-60 - (Oxycodone Hydrochloride and Acetaminophen)

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Drug Information of Oxycodone Hydrochloride and Acetaminophen

Product NDC: 42549-618
Proprietary Name: Oxycodone Hydrochloride and Acetaminophen
Non Proprietary Name: Oxycodone Hydrochloride and Acetaminophen
Active Ingredient(s): 325; 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 Hydrochloride and Acetaminophen

Product NDC: 42549-618
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040778
Marketing Category: ANDA
Start Marketing Date: 20080701

Package Information of Oxycodone Hydrochloride and Acetaminophen

Package NDC: 42549-618-60
Package Description: 60 TABLET in 1 BOTTLE (42549-618-60)

NDC Information of Oxycodone Hydrochloride and Acetaminophen

NDC Code 42549-618-60
Proprietary Name Oxycodone Hydrochloride and Acetaminophen
Package Description 60 TABLET in 1 BOTTLE (42549-618-60)
Product NDC 42549-618
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080701
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride and Acetaminophen


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