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Oxycodone Hydrochloride and Acetaminophen - 60760-200-92 - (Oxycodone Hydrochloride and Acetaminophen)

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Drug Information of Oxycodone Hydrochloride and Acetaminophen

Product NDC: 60760-200
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: 60760-200
Labeler Name: St. Mary's Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040777
Marketing Category: ANDA
Start Marketing Date: 20090608

Package Information of Oxycodone Hydrochloride and Acetaminophen

Package NDC: 60760-200-92
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (60760-200-92)

NDC Information of Oxycodone Hydrochloride and Acetaminophen

NDC Code 60760-200-92
Proprietary Name Oxycodone Hydrochloride and Acetaminophen
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (60760-200-92)
Product NDC 60760-200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090608
Marketing Category Name ANDA
Labeler Name St. Mary's Medical Park Pharmacy
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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