Package 72205-105-91
Brand: chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloridePackage Facts
Identity
Package NDC
72205-105-91
Digits Only
7220510591
Product NDC
72205-105
Description
100 TABLET, SUGAR COATED in 1 BOTTLE (72205-105-91)
Marketing
Marketing Status
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": "315ce03f-d9f8-4f3a-9e83-922747430c23", "openfda": {"upc": ["0372205106918", "0372205105911", "0372205104914", "0372205107915"], "unii": ["9WP59609J6"], "rxcui": ["991044", "991188", "991194", "991336"], "spl_set_id": ["315ce03f-d9f8-4f3a-9e83-922747430c23"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, SUGAR COATED in 1 BOTTLE (72205-105-91)", "package_ndc": "72205-105-91", "marketing_start_date": "20220209"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "72205-105_315ce03f-d9f8-4f3a-9e83-922747430c23", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72205-105", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214827", "marketing_category": "ANDA", "marketing_start_date": "20220209", "listing_expiration_date": "20261231"}