Package 62135-938-90
Brand: thioridazine hydrochloride
Generic: thioridazine hydrochloridePackage Facts
Identity
Package NDC
62135-938-90
Digits Only
6213593890
Product NDC
62135-938
Description
90 TABLET, FILM COATED in 1 BOTTLE (62135-938-90)
Marketing
Marketing Status
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 (62135-938-90)", "package_ndc": "62135-938-90", "marketing_start_date": "20250214"}], "brand_name": "Thioridazine Hydrochloride", "product_id": "62135-938_2e81bd7d-c434-2d02-e063-6294a90a196d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62135-938", "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": "50 mg/1"}], "application_number": "ANDA088134", "marketing_category": "ANDA", "marketing_start_date": "19830830", "listing_expiration_date": "20261231"}