Package 59651-570-99

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-570-99
Digits Only 5965157099
Product NDC 59651-570
Description

1000 TABLET in 1 BOTTLE (59651-570-99)

Marketing

Marketing Status
Marketed Since 2025-04-25
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb56a819-e085-4c21-a65e-4b685bde6f3e", "openfda": {"upc": ["0359651568019"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["c2a8b8a3-187f-4000-bde3-b40bb0e5600f"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-570-01)", "package_ndc": "59651-570-01", "marketing_start_date": "20250425"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59651-570-99)", "package_ndc": "59651-570-99", "marketing_start_date": "20250425"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "59651-570_eb56a819-e085-4c21-a65e-4b685bde6f3e", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "59651-570", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA216788", "marketing_category": "ANDA", "marketing_start_date": "20250425", "listing_expiration_date": "20261231"}