Home > National Drug Code (NDC) > Extra Strength QPAP

Extra Strength QPAP - 0603-0268-32 - (Acetaminophen)

Alphabetical Index


Drug Information of Extra Strength QPAP

Product NDC: 0603-0268
Proprietary Name: Extra Strength QPAP
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Extra Strength QPAP

Product NDC: 0603-0268
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110602

Package Information of Extra Strength QPAP

Package NDC: 0603-0268-32
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (0603-0268-32)

NDC Information of Extra Strength QPAP

NDC Code 0603-0268-32
Proprietary Name Extra Strength QPAP
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (0603-0268-32)
Product NDC 0603-0268
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110602
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Qualitest Pharmaceuticals
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Extra Strength QPAP


General Information