Package 62135-952-90
Brand: meclizine hydrochloride
Generic: meclizine hydrochloridePackage Facts
Identity
Package NDC
62135-952-90
Digits Only
6213595290
Product NDC
62135-952
Description
90 TABLET, FILM COATED in 1 BOTTLE (62135-952-90)
Marketing
Marketing Status
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": "90 TABLET, FILM COATED in 1 BOTTLE (62135-952-90)", "package_ndc": "62135-952-90", "marketing_start_date": "20250304"}], "brand_name": "Meclizine Hydrochloride", "product_id": "62135-952_30511729-d20f-8726-e063-6394a90a6053", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "62135-952", "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": "12.5 mg/1"}], "application_number": "ANDA203003", "marketing_category": "ANDA", "marketing_start_date": "20220811", "listing_expiration_date": "20261231"}