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Oxycodone and Acetaminophen - 47781-230-01 - (Oxycodone and Acetaminophen)

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Drug Information of Oxycodone and Acetaminophen

Product NDC: 47781-230
Proprietary Name: Oxycodone and Acetaminophen
Non Proprietary Name: Oxycodone and Acetaminophen
Active Ingredient(s): 325; 10    mg/1; mg/1 & nbsp;   Oxycodone and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone and Acetaminophen

Product NDC: 47781-230
Labeler Name: Alvogen, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202677
Marketing Category: ANDA
Start Marketing Date: 20120802

Package Information of Oxycodone and Acetaminophen

Package NDC: 47781-230-01
Package Description: 100 TABLET in 1 BOTTLE (47781-230-01)

NDC Information of Oxycodone and Acetaminophen

NDC Code 47781-230-01
Proprietary Name Oxycodone and Acetaminophen
Package Description 100 TABLET in 1 BOTTLE (47781-230-01)
Product NDC 47781-230
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120802
Marketing Category Name ANDA
Labeler Name Alvogen, Inc.
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 325; 10
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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