Home > National Drug Code (NDC) > Propoxyphene

Propoxyphene - 55289-324-20 - (Propoxyphene Hydrochloride)

Alphabetical Index


Drug Information of Propoxyphene

Product NDC: 55289-324
Proprietary Name: Propoxyphene
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

Product NDC: 55289-324
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083501
Marketing Category: ANDA
Start Marketing Date: 19730620

Package Information of Propoxyphene

Package NDC: 55289-324-20
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-324-20)

NDC Information of Propoxyphene

NDC Code 55289-324-20
Proprietary Name Propoxyphene
Package Description 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-324-20)
Product NDC 55289-324
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propoxyphene Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19730620
Marketing Category Name ANDA
Labeler Name PD-Rx 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


General Information