meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-953
Product ID 62135-953_30511729-d20f-8726-e063-6394a90a6053
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203003
Listing Expiration 2026-12-31
Marketing Start 2022-08-11

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135953
Hyphenated Format 62135-953

Supplemental Identifiers

RxCUI
995624 995666 995686
UPC
0362135954604 0362135952907 0362135953904
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 hydrochloride (source: ndc)
Generic Name meclizine hydrochloride (source: ndc)
Application Number ANDA203003 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (62135-953-90)
source: ndc

Packages (1)

62135-953-90 90 TABLET, FILM COATED in 1 BOTTLE (62135-953-90)

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": "30511729-d20f-8726-e063-6394a90a6053", "openfda": {"upc": ["0362135954604", "0362135952907", "0362135953904"], "unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666", "995686"], "spl_set_id": ["87d4c6d8-9218-48c2-9163-615a32449f11"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-953-90)", "package_ndc": "62135-953-90", "marketing_start_date": "20250304"}], "brand_name": "Meclizine Hydrochloride", "product_id": "62135-953_30511729-d20f-8726-e063-6394a90a6053", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "62135-953", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA203003", "marketing_category": "ANDA", "marketing_start_date": "20220811", "listing_expiration_date": "20261231"}