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PROPOXYPHENE HYDROCHLORIDE - 23155-012-05 - (propoxyphene hydrochloride)

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Drug Information of PROPOXYPHENE HYDROCHLORIDE

Product NDC: 23155-012
Proprietary Name: PROPOXYPHENE HYDROCHLORIDE
Non Proprietary Name: propoxyphene hydrochloride
Active Ingredient(s): 65    mg/1 & nbsp;   propoxyphene hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of PROPOXYPHENE HYDROCHLORIDE

Product NDC: 23155-012
Labeler Name: Heritage Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080530
Marketing Category: ANDA
Start Marketing Date: 20090501

Package Information of PROPOXYPHENE HYDROCHLORIDE

Package NDC: 23155-012-05
Package Description: 500 CAPSULE in 1 BOTTLE (23155-012-05)

NDC Information of PROPOXYPHENE HYDROCHLORIDE

NDC Code 23155-012-05
Proprietary Name PROPOXYPHENE HYDROCHLORIDE
Package Description 500 CAPSULE in 1 BOTTLE (23155-012-05)
Product NDC 23155-012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propoxyphene hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090501
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc
Substance Name PROPOXYPHENE HYDROCHLORIDE
Strength Number 65
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of PROPOXYPHENE HYDROCHLORIDE


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