Package 50268-163-15

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package 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
Marketed Since 2020-02-14
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"}