NDC 57344-170

Acetaminophen Rapid Release

Acetaminophen

Acetaminophen Rapid Release is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Aaa Pharmaceutical, Inc.. The primary component is Acetaminophen.

Product ID57344-170_92511556-01bb-4643-e053-2995a90a7dd8
NDC57344-170
Product TypeHuman Otc Drug
Proprietary NameAcetaminophen Rapid Release
Generic NameAcetaminophen
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2015-01-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameAAA Pharmaceutical, Inc.
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 57344-170-01

1 BOTTLE, PLASTIC in 1 CARTON (57344-170-01) > 24 TABLET, COATED in 1 BOTTLE, PLASTIC
Marketing Start Date2017-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57344-170-01 [57344017001]

Acetaminophen Rapid Release TABLET, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-09-01

NDC 57344-170-02 [57344017002]

Acetaminophen Rapid Release TABLET, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01

NDC 57344-170-04 [57344017004]

Acetaminophen Rapid Release TABLET, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Marketing End Date2019-09-11

NDC 57344-170-03 [57344017003]

Acetaminophen Rapid Release TABLET, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-09-01

NDC 57344-170-05 [57344017005]

Acetaminophen Rapid Release TABLET, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Marketing End Date2019-09-11

NDC 57344-170-12 [57344017012]

Acetaminophen Rapid Release TABLET, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-10-01

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:a891896d-c9fa-4448-915a-e6b531157d22
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • NDC Crossover Matching brand name "Acetaminophen Rapid Release" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    57344-170Acetaminophen Rapid ReleaseAcetaminophen Rapid Release
    61715-101Acetaminophen Rapid ReleaseAcetaminophen Rapid Release
    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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