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Propoxyphene Napsylate and Acetaminophen - 63629-1344-1 - (propoxyphene napsylate and acetaminophen)

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Drug Information of Propoxyphene Napsylate and Acetaminophen

Product NDC: 63629-1344
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: 63629-1344
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070145
Marketing Category: ANDA
Start Marketing Date: 20091104

Package Information of Propoxyphene Napsylate and Acetaminophen

Package NDC: 63629-1344-1
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (63629-1344-1)

NDC Information of Propoxyphene Napsylate and Acetaminophen

NDC Code 63629-1344-1
Proprietary Name Propoxyphene Napsylate and Acetaminophen
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (63629-1344-1)
Product NDC 63629-1344
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 20091104
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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