NDC 48083-310

CERTI-CET PLUS Extra Strength

Acetaminophen

CERTI-CET PLUS Extra Strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Certified Safety Manufacturing. The primary component is Acetaminophen.

Product ID48083-310_161cea83-fb45-4276-822a-14d2d2fa71a1
NDC48083-310
Product TypeHuman Otc Drug
Proprietary NameCERTI-CET PLUS Extra Strength
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-12-29
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameCertified Safety Manufacturing
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 48083-310-31

50 POUCH in 1 BOX (48083-310-31) > 2 TABLET in 1 POUCH
Marketing Start Date2017-12-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48083-310-27 [48083031027]

CERTI-CET PLUS Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-310-33 [48083031033]

CERTI-CET PLUS Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-310-36 [48083031036]

CERTI-CET PLUS Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-310-31 [48083031031]

CERTI-CET PLUS Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-310-30 [48083031030]

CERTI-CET PLUS Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

NDC 48083-310-39 [48083031039]

CERTI-CET PLUS Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-29
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:dcca9568-8eb5-4d70-a312-e6e1082f9972
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • UPC Code
  • 0766588040455
  • NDC Crossover Matching brand name "CERTI-CET PLUS Extra Strength" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    48083-310CERTI-CET PLUS Extra StrengthCERTI-CET PLUS Extra Strength
    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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