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Oxycodone and Acetaminophen - 42858-102-01 - (Oxycodone and Acetaminophen)

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Drug Information of Oxycodone and Acetaminophen

Product NDC: 42858-102
Proprietary Name: Oxycodone and Acetaminophen
Non Proprietary Name: Oxycodone and Acetaminophen
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   Oxycodone and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone and Acetaminophen

Product NDC: 42858-102
Labeler Name: Rhodes Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201278
Marketing Category: ANDA
Start Marketing Date: 20110811

Package Information of Oxycodone and Acetaminophen

Package NDC: 42858-102-01
Package Description: 100 TABLET, COATED in 1 BOTTLE, PLASTIC (42858-102-01)

NDC Information of Oxycodone and Acetaminophen

NDC Code 42858-102-01
Proprietary Name Oxycodone and Acetaminophen
Package Description 100 TABLET, COATED in 1 BOTTLE, PLASTIC (42858-102-01)
Product NDC 42858-102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone and Acetaminophen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20110811
Marketing Category Name ANDA
Labeler Name Rhodes Pharmaceuticals
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 and Acetaminophen


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