meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-237
Product ID 72189-237_15ac00f8-da4e-6cea-e063-6294a90aeb81
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA010721
Listing Expiration 2026-12-31
Marketing Start 2022-09-01

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189237
Hyphenated Format 72189-237

Supplemental Identifiers

RxCUI
995666
UNII
HDP7W44CIO

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 hydrochloride (source: ndc)
Generic Name meclizine hydrochloride (source: ndc)
Application Number NDA010721 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-237-30)
  • 90 TABLET in 1 BOTTLE (72189-237-90)
source: ndc

Packages (2)

72189-237-30 30 TABLET in 1 BOTTLE (72189-237-30) 72189-237-90 90 TABLET in 1 BOTTLE (72189-237-90)

Ingredients (1)

meclizine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Meclizine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "15ac00f8-da4e-6cea-e063-6294a90aeb81", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["e79ecf77-0e0a-d7ef-e053-2a95a90a5adf"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-237-30)", "package_ndc": "72189-237-30", "marketing_start_date": "20220901"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-237-90)", "package_ndc": "72189-237-90", "marketing_start_date": "20220901"}], "brand_name": "Meclizine Hydrochloride", "product_id": "72189-237_15ac00f8-da4e-6cea-e063-6294a90aeb81", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "72189-237", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "NDA010721", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}