Package 64950-268-10

Brand: clemastine fumarate

Generic: clemastine fumarate
NDC Package

Package Facts

Identity

Package NDC 64950-268-10
Digits Only 6495026810
Product NDC 64950-268
Description

100 TABLET in 1 BOTTLE (64950-268-10)

Marketing

Marketing Status
Marketed Since 2024-11-20
Brand clemastine fumarate
Generic clemastine fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "813d92a9-7e67-455e-9158-6aa5af5b27a7", "openfda": {"unii": ["19259EGQ3D"], "rxcui": ["857461"], "spl_set_id": ["cf8a3449-8bb3-4d5c-8d0d-557590e49ee5"], "manufacturer_name": ["Genus Lifesciences"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (64950-268-03)", "package_ndc": "64950-268-03", "marketing_start_date": "20241120"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (64950-268-10)", "package_ndc": "64950-268-10", "marketing_start_date": "20241120"}], "brand_name": "Clemastine Fumarate", "product_id": "64950-268_813d92a9-7e67-455e-9158-6aa5af5b27a7", "dosage_form": "TABLET", "product_ndc": "64950-268", "generic_name": "Clemastine Fumarate", "labeler_name": "Genus Lifesciences", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clemastine Fumarate", "active_ingredients": [{"name": "CLEMASTINE FUMARATE", "strength": "2.68 mg/1"}], "application_number": "ANDA073283", "marketing_category": "ANDA", "marketing_start_date": "20241120", "listing_expiration_date": "20261231"}