NDC 71335-0615

Meclizine HCL 12.5 mg

Meclizine Hcl 12.5 Mg

Meclizine HCL 12.5 mg is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Meclizine Hydrochloride.

Product ID71335-0615_bca52d3e-ddf2-43a6-8c68-22a2c511b998
NDC71335-0615
Product TypeHuman Otc Drug
Proprietary NameMeclizine HCL 12.5 mg
Generic NameMeclizine Hcl 12.5 Mg
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-11-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart336
Labeler NameBryant Ranch Prepack
Substance NameMECLIZINE HYDROCHLORIDE
Active Ingredient Strength13 mg/1
Pharm ClassesAntiemetic [EPC], Emesis Suppression [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-0615-1

30 TABLET in 1 BOTTLE (71335-0615-1)
Marketing Start Date2022-02-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0615-7 [71335061507]

Meclizine HCL 12.5 mg TABLET
Marketing CategoryOTC monograph final
Application Numberpart336
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-01
Marketing End Date2019-06-30

NDC 71335-0615-4 [71335061504]

Meclizine HCL 12.5 mg TABLET
Marketing CategoryOTC monograph final
Application Numberpart336
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-01
Marketing End Date2019-06-30

NDC 71335-0615-1 [71335061501]

Meclizine HCL 12.5 mg TABLET
Marketing CategoryOTC monograph final
Application Numberpart336
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-01
Marketing End Date2019-06-30

NDC 71335-0615-2 [71335061502]

Meclizine HCL 12.5 mg TABLET
Marketing CategoryOTC monograph final
Application Numberpart336
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-01
Marketing End Date2019-06-30

NDC 71335-0615-5 [71335061505]

Meclizine HCL 12.5 mg TABLET
Marketing CategoryOTC monograph final
Application Numberpart336
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-01
Marketing End Date2019-06-30

NDC 71335-0615-6 [71335061506]

Meclizine HCL 12.5 mg TABLET
Marketing CategoryOTC monograph final
Application Numberpart336
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-01
Marketing End Date2019-06-30

NDC 71335-0615-3 [71335061503]

Meclizine HCL 12.5 mg TABLET
Marketing CategoryOTC monograph final
Application Numberpart336
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-01
Marketing End Date2019-06-30

Drug Details

Active Ingredients

IngredientStrength
MECLIZINE HYDROCHLORIDE12.5 mg/1

OpenFDA Data

SPL SET ID:98c64895-50dc-45e8-ab70-04c5684ce6e0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 995624

    • NDC Crossover Matching brand name "Meclizine HCL 12.5 mg" or generic name "Meclizine Hcl 12.5 Mg"

    NDCBrand NameGeneric Name
    17714-117Meclizine HCL 12.5 mgMeclizine HCL 12.5 mg
    51655-428Meclizine HCL 12.5 mgMeclizine HCL 12.5 mg
    53002-6060Meclizine HCL 12.5 mgMeclizine HCL 12.5 mg
    68788-6956Meclizine HCL 12.5 mgMeclizine HCL 12.5 mg
    69618-027Meclizine HCL 12.5 mgMeclizine HCL 12.5 mg
    70934-196Meclizine HCL 12.5 mgMeclizine HCL 12.5 mg
    71335-0615Meclizine HCL 12.5 mgMeclizine HCL 12.5 mg
    0536-1297MECLIZINEMeclizine HCl 12.5 mg
    16103-386MECLIZINEMeclizine HCl 12.5 mg
    50090-3017MECLIZINEMeclizine HCl 12.5 mg
    66424-386MECLIZINEMeclizine HCl 12.5 mg
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