meclizine hcl 12.5 mg

Generic: meclizine hcl 12.5 mg

Labeler: advance pharmaceutical inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hcl 12.5 mg
Generic Name meclizine hcl 12.5 mg
Labeler advance pharmaceutical inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 12.5 mg/1

Manufacturer
Advance Pharmaceutical Inc.

Identifiers & Regulatory

Product NDC 17714-117
Product ID 17714-117_5cc9755e-6d41-fa9f-e053-2991aa0afbef
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part336
Listing Expiration 2026-12-31
Marketing Start 2013-07-01

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 17714117
Hyphenated Format 17714-117

Supplemental Identifiers

RxCUI
995624
UNII
HDP7W44CIO

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name meclizine hcl 12.5 mg (source: ndc)
Generic Name meclizine hcl 12.5 mg (source: ndc)
Application Number part336 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (17714-117-01)
source: ndc

Packages (1)

17714-117-01 100 TABLET in 1 BOTTLE (17714-117-01)

Ingredients (1)

meclizine hydrochloride (12.5 mg/1)

Linked Drug Pages (1)

Meclizine HCL 12.5 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5cc9755e-6d41-fa9f-e053-2991aa0afbef", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["76efad7e-e765-430f-9232-63553d02f2c5"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-117-01)", "package_ndc": "17714-117-01", "marketing_start_date": "20130701"}], "brand_name": "Meclizine HCL 12.5 mg", "product_id": "17714-117_5cc9755e-6d41-fa9f-e053-2991aa0afbef", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "17714-117", "generic_name": "Meclizine HCL 12.5 mg", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine HCL 12.5 mg", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "part336", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20130701", "listing_expiration_date": "20261231"}