meclizine hydrochloride

Generic: meclizine

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

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine
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 50090-7417
Product ID 50090-7417_129bad2d-36ae-482f-a8b0-a574d738216c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202640
Listing Expiration 2026-12-31
Marketing Start 2023-09-14

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907417
Hyphenated Format 50090-7417

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 (source: ndc)
Application Number ANDA202640 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (50090-7417-0)
  • 30 TABLET in 1 BOTTLE (50090-7417-1)
  • 10 TABLET in 1 BOTTLE (50090-7417-4)
  • 90 TABLET in 1 BOTTLE (50090-7417-8)
source: ndc

Packages (4)

50090-7417-0 20 TABLET in 1 BOTTLE (50090-7417-0) 50090-7417-1 30 TABLET in 1 BOTTLE (50090-7417-1) 50090-7417-4 10 TABLET in 1 BOTTLE (50090-7417-4) 50090-7417-8 90 TABLET in 1 BOTTLE (50090-7417-8)

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": "129bad2d-36ae-482f-a8b0-a574d738216c", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["55e262d9-d9dd-43a3-bc74-35e46dd391be"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-7417-0)", "package_ndc": "50090-7417-0", "marketing_start_date": "20241028"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7417-1)", "package_ndc": "50090-7417-1", "marketing_start_date": "20241028"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-7417-4)", "package_ndc": "50090-7417-4", "marketing_start_date": "20241028"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7417-8)", "package_ndc": "50090-7417-8", "marketing_start_date": "20241028"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "50090-7417_129bad2d-36ae-482f-a8b0-a574d738216c", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "50090-7417", "generic_name": "MECLIZINE", "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": "ANDA202640", "marketing_category": "ANDA", "marketing_start_date": "20230914", "listing_expiration_date": "20261231"}