NDC 11673-437

up and up acetaminophen pm extra strength

Acetaminophen, Diphenhydramine Hcl

up and up acetaminophen pm extra strength is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.

Product ID11673-437_4fda27e0-6981-42e0-bf63-bf35c1e898cf
NDC11673-437
Product TypeHuman Otc Drug
Proprietary Nameup and up acetaminophen pm extra strength
Generic NameAcetaminophen, Diphenhydramine Hcl
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2009-06-26
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameTarget Corporation
Substance NameACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength500 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 11673-437-47

1 BOTTLE in 1 CARTON (11673-437-47) > 150 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2017-04-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-437-62 [11673043762]

up and up acetaminophen pm extra strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-04-29

NDC 11673-437-71 [11673043771]

up and up acetaminophen pm extra strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-06-26

NDC 11673-437-47 [11673043747]

up and up acetaminophen pm extra strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-04-29

NDC 11673-437-78 [11673043778]

up and up acetaminophen pm extra strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-07-10

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:f1a10eba-0baa-4e34-bfbe-69faed6b51f1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1092189

    • NDC Crossover Matching brand name "up and up acetaminophen pm extra strength" or generic name "Acetaminophen, Diphenhydramine Hcl"

    NDCBrand NameGeneric Name
    11673-556Acetaminophen PMAcetaminophen, Diphenhydramine HCl
    21130-360Acetaminophen PMAcetaminophen, Diphenhydramine HCl
    30142-530acetaminophen pmAcetaminophen, Diphenhydramine HCl
    30142-700acetaminophen pmAcetaminophen, Diphenhydramine HCl
    30142-800acetaminophen pmAcetaminophen, Diphenhydramine HCl
    0113-7437basic care acetaminophen PMAcetaminophen, Diphenhydramine HCl
    0113-0355Good Sense headache pmAcetaminophen, Diphenhydramine HCl
    0113-0437good sense pain relief pmAcetaminophen, Diphenhydramine HCl
    0113-0837Good Sense Pain Relief PMAcetaminophen, Diphenhydramine HCl
    0363-0246Pain Relief PMAcetaminophen, Diphenhydramine HCl
    33992-0213Pain Relief PMAcetaminophen, Diphenhydramine HCl
    33992-0447Pain Relief PMAcetaminophen, Diphenhydramine HCl
    36800-229Pain Relief PMAcetaminophen, Diphenhydramine HCl
    15127-898Pain RelieverAcetaminophen, Diphenhydramine HCl
    0363-0213Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-0350PAIN RELIEVER PMAcetaminophen, Diphenhydramine HCl
    0363-0556Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-0760Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-0863Pain Reliever PMAcetaminophen, Diphenhydramine HCL
    0363-2035Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-4470Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-9074Sleep Aid Plus Pain ReliefAcetaminophen, Diphenhydramine HCl
    11673-437up and up acetaminophen pmAcetaminophen, Diphenhydramine HCl
    0363-7400Wal-Sleep Z Pain ReliefACETAMINOPHEN, DIPHENHYDRAMINE HCl
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