Package 50268-163-15
Brand: chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloridePackage Facts
Identity
Package NDC
50268-163-15
Digits Only
5026816315
Product NDC
50268-163
Description
50 BLISTER PACK in 1 BOX (50268-163-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-163-11)
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": "47e24518-b486-ad20-e063-6294a90ad040", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["9e8cebc0-7fcf-dca8-e053-2a95a90a3369"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-163-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-163-11)", "package_ndc": "50268-163-15", "marketing_start_date": "20200214"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "50268-163_47e24518-b486-ad20-e063-6294a90ad040", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50268-163", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA209755", "marketing_category": "ANDA", "marketing_start_date": "20200214", "listing_expiration_date": "20271231"}