Package 0781-4027-53

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0781-4027-53
Digits Only 0781402753
Product NDC 0781-4027
Product ID 0781-4027_cfff95df-4926-4139-a109-2beebebcf014
Description

120 mL in 1 BOTTLE, PLASTIC (0781-4027-53)

Marketing

Marketing Status
Marketed Since 2023-03-31
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": "cfff95df-4926-4139-a109-2beebebcf014", "openfda": {"upc": ["0307814028221", "0307814027538"], "unii": ["9WP59609J6"], "rxcui": ["991053", "991332"], "spl_set_id": ["9398a0b4-e08b-4eb7-9f31-97d4f384427a"], "manufacturer_name": ["Sandoz, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE, PLASTIC (0781-4027-53)", "package_ndc": "0781-4027-53", "marketing_start_date": "20230331"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "0781-4027_cfff95df-4926-4139-a109-2beebebcf014", "dosage_form": "CONCENTRATE", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0781-4027", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Sandoz, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "30 mg/mL"}], "application_number": "ANDA214542", "marketing_category": "ANDA", "marketing_start_date": "20230331", "listing_expiration_date": "20261231"}