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Oxycodone and Acetaminophen - 10544-621-10 - (Oxycodone and Acetaminophen)

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Drug Information of Oxycodone and Acetaminophen

Product NDC: 10544-621
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
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone and Acetaminophen

Product NDC: 10544-621
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040777
Marketing Category: ANDA
Start Marketing Date: 20100517

Package Information of Oxycodone and Acetaminophen

Package NDC: 10544-621-10
Package Description: 10 TABLET in 1 BOTTLE (10544-621-10)

NDC Information of Oxycodone and Acetaminophen

NDC Code 10544-621-10
Proprietary Name Oxycodone and Acetaminophen
Package Description 10 TABLET in 1 BOTTLE (10544-621-10)
Product NDC 10544-621
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100517
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name ACETAMINOPHEN; OXYCODONE
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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