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PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN - 67296-0104-1 - (propoxyphene napsylate and acetaminophen)

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Drug Information of PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product NDC: 67296-0104
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
Coding System: National Drug Codes(NDC)

Labeler Information of PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product NDC: 67296-0104
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075738
Marketing Category: ANDA
Start Marketing Date: 20090608

Package Information of PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Package NDC: 67296-0104-1
Package Description: 15 TABLET in 1 BOTTLE (67296-0104-1)

NDC Information of PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

NDC Code 67296-0104-1
Proprietary Name PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
Package Description 15 TABLET in 1 BOTTLE (67296-0104-1)
Product NDC 67296-0104
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propoxyphene napsylate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090608
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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