Package 69238-1058-1
Brand: chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloridePackage Facts
Identity
Package NDC
69238-1058-1
Digits Only
6923810581
Product NDC
69238-1058
Description
100 TABLET, FILM COATED in 1 BOTTLE (69238-1058-1)
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": "9e50c657-1fae-40c2-af7e-e3c389dd5a6d", "openfda": {"upc": ["0369238105612", "0369238106213"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["aa086a21-de85-4b03-af58-49b70acf8cf0"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69238-1058-1)", "package_ndc": "69238-1058-1", "marketing_start_date": "20180912"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "69238-1058_9e50c657-1fae-40c2-af7e-e3c389dd5a6d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "69238-1058", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA209755", "marketing_category": "ANDA", "marketing_start_date": "20180912", "listing_expiration_date": "20271231"}