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Propoxyphene Napsylate and Acetaminophen - 67296-0378-2 - (Propoxyphene Napsylate and Acetaminophen)

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Drug Information of Propoxyphene Napsylate and Acetaminophen

Product NDC: 67296-0378
Proprietary Name: Propoxyphene Napsylate and Acetaminophen
Non Proprietary Name: Propoxyphene Napsylate and Acetaminophen
Active Ingredient(s): 650; 100    mg/1; mg/1 & nbsp;   Propoxyphene Napsylate and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Propoxyphene Napsylate and Acetaminophen

Product NDC: 67296-0378
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074119
Marketing Category: ANDA
Start Marketing Date: 20091125

Package Information of Propoxyphene Napsylate and Acetaminophen

Package NDC: 67296-0378-2
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (67296-0378-2)

NDC Information of Propoxyphene Napsylate and Acetaminophen

NDC Code 67296-0378-2
Proprietary Name Propoxyphene Napsylate and Acetaminophen
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (67296-0378-2)
Product NDC 67296-0378
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propoxyphene Napsylate and Acetaminophen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091125
Marketing Category Name ANDA
Labeler Name RedPharm Drug Inc.
Substance Name ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Strength Number 650; 100
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Propoxyphene Napsylate and Acetaminophen


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