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Propoxyphene and Acetaminophen - 63874-201-60 - (propoxyphene napsylate and acetaminophen)

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Drug Information of Propoxyphene and Acetaminophen

Product NDC: 63874-201
Proprietary Name: Propoxyphene 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 and Acetaminophen

Product NDC: 63874-201
Labeler Name: Altura Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074843
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of Propoxyphene and Acetaminophen

Package NDC: 63874-201-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63874-201-60)

NDC Information of Propoxyphene and Acetaminophen

NDC Code 63874-201-60
Proprietary Name Propoxyphene and Acetaminophen
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63874-201-60)
Product NDC 63874-201
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 20100101
Marketing Category Name ANDA
Labeler Name Altura Pharmaceuticals, 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 and Acetaminophen


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