Package 62135-939-90

Brand: thioridazine hydrochloride

Generic: thioridazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-939-90
Digits Only 6213593990
Product NDC 62135-939
Description

90 TABLET, FILM COATED in 1 BOTTLE (62135-939-90)

Marketing

Marketing Status
Marketed Since 2025-02-14
Brand thioridazine hydrochloride
Generic thioridazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e81bd7d-c434-2d02-e063-6294a90a196d", "openfda": {"upc": ["0362135934903", "0362135936907", "0362135939908", "0362135938901"], "unii": ["4WCI67NK8M"], "rxcui": ["198270", "198274", "198275", "313354"], "spl_set_id": ["e0bbe982-6434-468b-bd29-64ac57386fbe"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-939-90)", "package_ndc": "62135-939-90", "marketing_start_date": "20250214"}], "brand_name": "Thioridazine Hydrochloride", "product_id": "62135-939_2e81bd7d-c434-2d02-e063-6294a90a196d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62135-939", "generic_name": "Thioridazine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thioridazine Hydrochloride", "active_ingredients": [{"name": "THIORIDAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA088135", "marketing_category": "ANDA", "marketing_start_date": "19841120", "listing_expiration_date": "20261231"}