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Oxycodone and Acetaminophen - 60760-933-60 - (OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN)

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Drug Information of Oxycodone and Acetaminophen

Product NDC: 60760-933
Proprietary Name: Oxycodone and Acetaminophen
Non Proprietary Name: OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Active Ingredient(s): 325; 7.5    mg/1; mg/1 & nbsp;   OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone and Acetaminophen

Product NDC: 60760-933
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040545
Marketing Category: ANDA
Start Marketing Date: 20101222

Package Information of Oxycodone and Acetaminophen

Package NDC: 60760-933-60
Package Description: 60 TABLET in 1 BOTTLE (60760-933-60)

NDC Information of Oxycodone and Acetaminophen

NDC Code 60760-933-60
Proprietary Name Oxycodone and Acetaminophen
Package Description 60 TABLET in 1 BOTTLE (60760-933-60)
Product NDC 60760-933
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101222
Marketing Category Name ANDA
Labeler Name St Marys Medical Park Pharmacy
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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