Package 65197-520-16

Brand: bonine max

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65197-520-16
Digits Only 6519752016
Product NDC 65197-520
Product ID 65197-520_610a37d5-4aa5-49cf-b50c-0ddda9d1d026
Description

2 BLISTER PACK in 1 BOX (65197-520-16) / 8 TABLET, CHEWABLE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-03-24
Brand bonine max
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

BONINE MAX ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "610a37d5-4aa5-49cf-b50c-0ddda9d1d026", "openfda": {"upc": ["0365197295203"], "unii": ["HDP7W44CIO"], "rxcui": ["2632643"], "spl_set_id": ["7326a47e-284e-4b6f-8eb0-7933dc1e3f0d"], "manufacturer_name": ["WellSpring Pharmaceutical Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 BOX (65197-520-16)  / 8 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "65197-520-16", "marketing_start_date": "20230324"}, {"sample": false, "description": "2 BLISTER PACK in 1 BOX (65197-520-17)  / 8 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "65197-520-17", "marketing_start_date": "20250415"}], "brand_name": "BONINE MAX", "product_id": "65197-520_610a37d5-4aa5-49cf-b50c-0ddda9d1d026", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "65197-520", "generic_name": "meclizine hydrochloride", "labeler_name": "WellSpring Pharmaceutical Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BONINE MAX", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230324", "listing_expiration_date": "20261231"}