NDC 50066-267

Bi Electro Extra Strength

Acetaminophen/diphenhydramine Hcl Caplets

Bi Electro Extra Strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Genomma Labs Usa, Inc. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.

Product ID50066-267_4ae1c5f3-fc79-45f4-91df-15d93965f31c
NDC50066-267
Product TypeHuman Otc Drug
Proprietary NameBi Electro Extra Strength
Generic NameAcetaminophen/diphenhydramine Hcl Caplets
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-12-23
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameGenomma Labs USA, Inc
Substance NameACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength500 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50066-267-24

1 BOTTLE in 1 CARTON (50066-267-24) > 24 TABLET in 1 BOTTLE
Marketing Start Date2014-12-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50066-267-24 [50066026724]

Bi Electro Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-12-23
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:1ae15feb-bd13-4aec-afc7-ff77de8b0256
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1092189
  • UPC Code
  • 0650066000058
  • NDC Crossover Matching brand name "Bi Electro Extra Strength" or generic name "Acetaminophen/diphenhydramine Hcl Caplets"

    NDCBrand NameGeneric Name
    50066-285Bi Electro Extra StrengthBi Electro Extra Strength
    50066-267Bi ElectroAcetaminophen/diphenhydramine HCL Caplets

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