NDC 36800-917

Topcare pain relief extra strength

Acetaminophen

Topcare pain relief extra strength is a Oral Capsule, Coated in the Human Otc Drug category. It is labeled and distributed by Topco Associates Llc. The primary component is Acetaminophen.

Product ID36800-917_5df591c3-1012-4c62-8ccf-f66ee9d9d598
NDC36800-917
Product TypeHuman Otc Drug
Proprietary NameTopcare pain relief extra strength
Generic NameAcetaminophen
Dosage FormCapsule, Coated
Route of AdministrationORAL
Marketing Start Date2011-01-05
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameTopco Associates LLC
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 36800-917-90

500 CAPSULE, COATED in 1 BOTTLE (36800-917-90)
Marketing Start Date2011-04-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36800-917-62 [36800091762]

Topcare pain relief extra strength CAPSULE, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-15
Marketing End Date2014-03-17

NDC 36800-917-71 [36800091771]

Topcare pain relief extra strength CAPSULE, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-10
Marketing End Date2014-02-26

NDC 36800-917-78 [36800091778]

Topcare pain relief extra strength CAPSULE, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-01-05
Marketing End Date2013-01-22

NDC 36800-917-90 [36800091790]

Topcare pain relief extra strength CAPSULE, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-06
Marketing End Date2014-03-03

NDC 36800-917-76 [36800091776]

Topcare pain relief extra strength CAPSULE, COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-07-18
Marketing End Date2014-02-26

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:77ef1e2e-b69f-4d2b-a369-017739c707f8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198439
  • NDC Crossover Matching brand name "Topcare pain relief extra strength" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    36800-917Topcare pain relief extra strengthTopcare pain relief 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.