meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5728
Product ID 50090-5728_154a8e7e-94cf-413f-9a2b-5f07b7bfa61c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213957
Listing Expiration 2026-12-31
Marketing Start 2020-10-29

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905728
Hyphenated Format 50090-5728

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 ANDA213957 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (50090-5728-0)
  • 30 TABLET in 1 BOTTLE (50090-5728-1)
  • 10 TABLET in 1 BOTTLE (50090-5728-4)
  • 90 TABLET in 1 BOTTLE (50090-5728-8)
source: ndc

Packages (4)

Ingredients (1)

meclizine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "154a8e7e-94cf-413f-9a2b-5f07b7bfa61c", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["eae4bc73-fee1-4831-b31c-8ca56fb83ad7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-5728-0)", "package_ndc": "50090-5728-0", "marketing_start_date": "20210928"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5728-1)", "package_ndc": "50090-5728-1", "marketing_start_date": "20210928"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-5728-4)", "package_ndc": "50090-5728-4", "marketing_start_date": "20210928"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5728-8)", "package_ndc": "50090-5728-8", "marketing_start_date": "20210928"}], "brand_name": "Meclizine Hydrochloride", "product_id": "50090-5728_154a8e7e-94cf-413f-9a2b-5f07b7bfa61c", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "50090-5728", "generic_name": "Meclizine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA213957", "marketing_category": "ANDA", "marketing_start_date": "20201029", "listing_expiration_date": "20261231"}