Package 51079-565-20

Brand: thioridazine hydrochloride

Generic: thioridazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51079-565-20
Digits Only 5107956520
Product NDC 51079-565
Description

100 BLISTER PACK in 1 CARTON (51079-565-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-565-01)

Marketing

Marketing Status
Marketed Since 1998-04-29
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": "4358c933-3022-792d-e063-6294a90aacb6", "openfda": {"unii": ["4WCI67NK8M"], "rxcui": ["198270", "198274", "198275", "313354"], "spl_set_id": ["52fea941-0b47-41c1-b00d-f88150e8ab93"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-565-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-565-01)", "package_ndc": "51079-565-20", "marketing_start_date": "19980429"}], "brand_name": "Thioridazine Hydrochloride", "product_id": "51079-565_4358c933-3022-792d-e063-6294a90aacb6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51079-565", "generic_name": "thioridazine hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thioridazine Hydrochloride", "active_ingredients": [{"name": "THIORIDAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088004", "marketing_category": "ANDA", "marketing_start_date": "19980429", "listing_expiration_date": "20261231"}