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Oxycodone Hydrochloride and Acetaminophen - 43063-025-12 - (Oxycodone Hydrochloride and Acetaminophen)

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Drug Information of Oxycodone Hydrochloride and Acetaminophen

Product NDC: 43063-025
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: 43063-025
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040777
Marketing Category: ANDA
Start Marketing Date: 20071127

Package Information of Oxycodone Hydrochloride and Acetaminophen

Package NDC: 43063-025-12
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC (43063-025-12)

NDC Information of Oxycodone Hydrochloride and Acetaminophen

NDC Code 43063-025-12
Proprietary Name Oxycodone Hydrochloride and Acetaminophen
Package Description 12 TABLET in 1 BOTTLE, PLASTIC (43063-025-12)
Product NDC 43063-025
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071127
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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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