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Regular Strength QPAP - 63629-1518-1 - (Acetaminophen)

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Drug Information of Regular Strength QPAP

Product NDC: 63629-1518
Proprietary Name: Regular Strength QPAP
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 325    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Regular Strength QPAP

Product NDC: 63629-1518
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19960201

Package Information of Regular Strength QPAP

Package NDC: 63629-1518-1
Package Description: 20 TABLET in 1 BOTTLE (63629-1518-1)

NDC Information of Regular Strength QPAP

NDC Code 63629-1518-1
Proprietary Name Regular Strength QPAP
Package Description 20 TABLET in 1 BOTTLE (63629-1518-1)
Product NDC 63629-1518
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Bryant Ranch Prepack
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Regular Strength QPAP


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