Package 60687-441-01

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-441-01
Digits Only 6068744101
Product NDC 60687-441
Product ID 60687-441_4342f33e-4430-7a74-e063-6294a90adba7
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-441-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-441-11)

Marketing

Marketing Status
Marketed Since 2019-05-16
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

CHLORPROMAZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4342f33e-4430-7a74-e063-6294a90adba7", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["d43718e5-66d7-44f9-9fc8-80d38d3e41ce"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-441-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-441-11)", "package_ndc": "60687-441-01", "marketing_start_date": "20190516"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "60687-441_4342f33e-4430-7a74-e063-6294a90adba7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "60687-441", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "American Health Packaging", "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": "20190516", "listing_expiration_date": "20261231"}