NDC 63629-1518

Regular Strength QPAP

Acetaminophen

Regular Strength QPAP is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Acetaminophen.

Product ID63629-1518_f11b14ce-1cc6-41eb-a037-cc5adca20f0f
NDC63629-1518
Product TypeHuman Prescription Drug
Proprietary NameRegular Strength QPAP
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1996-02-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameBryant Ranch Prepack
Substance NameACETAMINOPHEN
Active Ingredient Strength325 mg/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63629-1518-2

100 TABLET in 1 BOTTLE (63629-1518-2)
Marketing Start Date1996-02-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-1518-1 [63629151801]

Regular Strength QPAP TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1996-02-01
Inactivation Date2019-11-27

NDC 63629-1518-2 [63629151802]

Regular Strength QPAP TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1996-02-01
Inactivation Date2019-11-27

NDC 63629-1518-6 [63629151806]

Regular Strength QPAP TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-02-01
Inactivation Date2019-11-27

NDC 63629-1518-5 [63629151805]

Regular Strength QPAP TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-02-01
Inactivation Date2019-11-27

NDC 63629-1518-3 [63629151803]

Regular Strength QPAP TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1996-02-01
Inactivation Date2019-11-27

NDC 63629-1518-4 [63629151804]

Regular Strength QPAP TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1996-02-01
Inactivation Date2019-11-27

NDC 63629-1518-7 [63629151807]

Regular Strength QPAP TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1996-02-01
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN325 mg/1

OpenFDA Data

SPL SET ID:42e4219a-a4ef-f090-f6a4-2fd2e213d397
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313782
  • NDC Crossover Matching brand name "Regular Strength QPAP" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    63629-1518Regular Strength QPAPRegular 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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