Package 53489-149-10

Brand: thioridazine hydrochloride

Generic: thioridazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53489-149-10
Digits Only 5348914910
Product NDC 53489-149
Product ID 53489-149_2c96c6f9-3008-48ba-86ea-e9b83502da67
Description

1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-149-10)

Marketing

Marketing Status
Marketed Since 1988-10-07
Brand thioridazine hydrochloride
Generic thioridazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Thioridazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c96c6f9-3008-48ba-86ea-e9b83502da67", "openfda": {"unii": ["4WCI67NK8M"], "rxcui": ["198270", "198274", "198275", "313354"], "spl_set_id": ["9c4bedb4-2d59-4fcd-aad7-fce988cd96d8"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-149-01)", "package_ndc": "53489-149-01", "marketing_start_date": "19881007"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-149-10)", "package_ndc": "53489-149-10", "marketing_start_date": "19881007"}], "brand_name": "Thioridazine Hydrochloride", "product_id": "53489-149_2c96c6f9-3008-48ba-86ea-e9b83502da67", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "53489-149", "generic_name": "Thioridazine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thioridazine Hydrochloride", "active_ingredients": [{"name": "THIORIDAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA089953", "marketing_category": "ANDA", "marketing_start_date": "19881007", "listing_expiration_date": "20261231"}