Package 62135-954-60

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-954-60
Digits Only 6213595460
Product NDC 62135-954
Description

60 TABLET, FILM COATED in 1 BOTTLE (62135-954-60)

Marketing

Marketing Status
Marketed Since 2025-03-04
Brand meclizine hydrochloride
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

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": "60 TABLET, FILM COATED in 1 BOTTLE (62135-954-60)", "package_ndc": "62135-954-60", "marketing_start_date": "20250304"}], "brand_name": "Meclizine Hydrochloride", "product_id": "62135-954_30511729-d20f-8726-e063-6394a90a6053", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "62135-954", "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": "50 mg/1"}], "application_number": "ANDA203003", "marketing_category": "ANDA", "marketing_start_date": "20220811", "listing_expiration_date": "20261231"}