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Oxycodone and Acetaminophen - 21695-619-60 - (Oxycodone and Acetaminophen)

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Drug Information of Oxycodone and Acetaminophen

Product NDC: 21695-619
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: 21695-619
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040778
Marketing Category: ANDA
Start Marketing Date: 20071127

Package Information of Oxycodone and Acetaminophen

Package NDC: 21695-619-60
Package Description: 60 TABLET in 1 BOTTLE (21695-619-60)

NDC Information of Oxycodone and Acetaminophen

NDC Code 21695-619-60
Proprietary Name Oxycodone and Acetaminophen
Package Description 60 TABLET in 1 BOTTLE (21695-619-60)
Product NDC 21695-619
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071127
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name ACETAMINOPHEN; OXYCODONE
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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