NDC 57344-001

Acetaminophen

Acetaminophen

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

Product ID57344-001_7e55ec9f-3b0a-586c-e053-2a91aa0a7baf
NDC57344-001
Product TypeHuman Otc Drug
Proprietary NameAcetaminophen
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-12-13
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameAAA Pharmaceutical, Inc.
Substance NameACETAMINOPHEN
Active Ingredient Strength325 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 57344-001-02

1 BOTTLE, PLASTIC in 1 CARTON (57344-001-02) > 100 TABLET in 1 BOTTLE, PLASTIC
Marketing Start Date2012-12-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57344-001-04 [57344000104]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

NDC 57344-001-03 [57344000103]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

NDC 57344-001-07 [57344000107]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

NDC 57344-001-05 [57344000105]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

NDC 57344-001-08 [57344000108]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

NDC 57344-001-02 [57344000102]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

NDC 57344-001-06 [57344000106]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

NDC 57344-001-01 [57344000101]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

NDC 57344-001-99 [57344000199]

Acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-12-13
Marketing End Date2012-12-14

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN325 mg/1

OpenFDA Data

SPL SET ID:e9770104-0853-481c-a86c-5e1f6f6653dd
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313782

    • NDC Crossover Matching brand name "Acetaminophen" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    0121-0657AcetaminophenAcetaminophen
    68016-656AcetaminophenAcetaminophen
    68016-657AcetaminophenAcetaminophen
    68016-655AcetaminophenAcetaminophen
    68210-0022ACETAMINOPHENACETAMINOPHEN
    68210-0023ACETAMINOPHENACETAMINOPHEN
    68387-214ACETAMINOPHENACETAMINOPHEN
    0536-1172AcetaminophenAcetaminophen
    0536-3233AcetaminophenAcetaminophen
    69477-000AcetaminophenAcetaminophen
    69517-628AcetaminophenAcetaminophen
    69517-623AcetaminophenAcetaminophen
    69517-627AcetaminophenAcetaminophen
    69584-012AcetaminophenAcetaminophen
    69517-624AcetaminophenAcetaminophen
    69842-298AcetaminophenAcetaminophen
    69842-168acetaminophenacetaminophen
    69842-311AcetaminophenAcetaminophen
    69842-465AcetaminophenAcetaminophen
    69842-484acetaminophenacetaminophen
    69842-707acetaminophenacetaminophen
    69842-930AcetaminophenAcetaminophen
    70000-0153ACETAMINOPHENACETAMINOPHEN
    70000-0104AcetaminophenAcetaminophen
    70000-0152AcetaminophenAcetaminophen
    70000-0410AcetaminophenAcetaminophen
    70000-0151AcetaminophenAcetaminophen
    70000-0446AcetaminophenAcetaminophen
    70000-0150ACETAMINOPHENACETAMINOPHEN
    70518-1101ACETAMINOPHENACETAMINOPHEN
    70518-1915AcetaminophenAcetaminophen
    70518-1930AcetaminophenAcetaminophen
    70518-1840AcetaminophenAcetaminophen
    71141-004AcetaminophenAcetaminophen
    0615-0591AcetaminophenAcetaminophen
    71247-129AcetaminophenAcetaminophen
    71205-165AcetaminophenAcetaminophen
    0615-2542AcetaminophenAcetaminophen
    71321-100AcetaminophenAcetaminophen
    0615-4510AcetaminophenAcetaminophen
    0615-4554AcetaminophenAcetaminophen
    71610-238AcetaminophenAcetaminophen
    76168-010AcetaminophenAcetaminophen
    72570-100AcetaminophenAcetaminophen
    76168-120AcetaminophenAcetaminophen
    76413-301AcetaminophenAcetaminophen
    0615-8250AcetaminophenAcetaminophen
    0904-6749AcetaminophenAcetaminophen
    0904-6719AcetaminophenAcetaminophen
    0904-6720acetaminophenacetaminophen

    Trademark Results [Acetaminophen]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ACETAMINOPHEN
    ACETAMINOPHEN
    85615223 not registered Dead/Abandoned
    General Merchandise importers and Expoters
    2012-05-03
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.