NDC 68788-9196

Extra Strength QPAP

Acetaminophen

Extra Strength QPAP is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is Acetaminophen.

Product ID68788-9196_5307263a-f3d0-4afd-afba-8c27617ed23c
NDC68788-9196
Product TypeHuman Otc Drug
Proprietary NameExtra Strength QPAP
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2011-11-03
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-9196-3

30 TABLET in 1 BOTTLE, PLASTIC (68788-9196-3)
Marketing Start Date2011-11-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9196-4 [68788919604]

Extra Strength QPAP TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-11-03
Marketing End Date2019-09-16

NDC 68788-9196-1 [68788919601]

Extra Strength QPAP TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-11-03
Marketing End Date2019-09-16

NDC 68788-9196-3 [68788919603]

Extra Strength QPAP TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-11-03
Marketing End Date2019-09-16

NDC 68788-9196-2 [68788919602]

Extra Strength QPAP TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-11-03
Marketing End Date2019-09-16

NDC 68788-9196-5 [68788919605]

Extra Strength QPAP TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-11-03
Marketing End Date2019-09-16

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:beb90934-9ec4-4bb4-90a4-29d17cacc4e8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • NDC Crossover Matching brand name "Extra Strength QPAP" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    68788-9196Extra Strength QPAPExtra Strength QPAP
    0121-0657AcetaminophenAcetaminophen
    0113-7000Basic Care acetaminophenAcetaminophen
    0113-7484basic care acetaminophenAcetaminophen
    0113-7544Basic Care AcetaminophenAcetaminophen
    0113-7130basic care childrens pain and feverAcetaminophen
    0113-0020good sense childrens pain and feverAcetaminophen
    0113-0212Good Sense Childrens Pain and FeverAcetaminophen
    0113-0608good sense childrens pain and feverAcetaminophen
    0113-0998Good Sense Childrens Pain and FeverAcetaminophen
    0113-0161Good Sense pain and feverAcetaminophen
    0113-0397Good Sense Pain and Feveracetaminophen
    0113-0590Good Sense Pain and Feveracetaminophen
    0113-0946good sense pain and feverAcetaminophen
    0113-8959Good Sense Pain and FeverAcetaminophen
    0113-0025Good Sense Pain ReliefAcetaminophen
    0113-0044Good Sense Pain ReliefAcetaminophen
    0113-0187good sense pain reliefAcetaminophen
    0113-0217good sense pain reliefAcetaminophen
    0113-0227Good Sense Pain ReliefAcetaminophen
    0113-0403good sense pain reliefAcetaminophen
    0113-0484Good Sense Pain ReliefAcetaminophen
    0113-0518good sense pain reliefAcetaminophen
    0113-0544good sense pain reliefAcetaminophen
    0113-1889good sense pain reliefacetaminophen
    0113-1975Good Sense Pain ReliefAcetaminophen
    0031-9301Robitussin Direct Sore Throat Painacetaminophen

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