Package 63304-114-01

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine
NDC Package

Package Facts

Identity

Package NDC 63304-114-01
Digits Only 6330411401
Product NDC 63304-114
Description

100 TABLET, SUGAR COATED in 1 BOTTLE (63304-114-01)

Marketing

Marketing Status
Marketed Since 2020-11-18
Brand chlorpromazine hydrochloride
Generic chlorpromazine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c2d3824b-8e6f-414d-aa16-de9e2d448645", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["432cd4ca-c728-48ff-beec-2485f5e02512"], "manufacturer_name": ["Sun Pharmaceutical Industries Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, SUGAR COATED in 1 BOTTLE (63304-114-01)", "package_ndc": "63304-114-01", "marketing_start_date": "20201118"}, {"sample": false, "description": "1000 TABLET, SUGAR COATED in 1 BOTTLE (63304-114-10)", "package_ndc": "63304-114-10", "marketing_start_date": "20201118"}], "brand_name": "ChlorproMAZINE Hydrochloride", "product_id": "63304-114_c2d3824b-8e6f-414d-aa16-de9e2d448645", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "63304-114", "generic_name": "ChlorproMAZINE", "labeler_name": "Sun Pharmaceutical Industries Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ChlorproMAZINE Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA214256", "marketing_category": "ANDA", "marketing_start_date": "20201118", "listing_expiration_date": "20261231"}