Package 65219-130-02

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65219-130-02
Digits Only 6521913002
Product NDC 65219-130
Product ID 65219-130_64ba1614-82e8-476f-957d-a29198c7a26e
Description

25 VIAL in 1 CARTON (65219-130-02) / 2 mL in 1 VIAL (65219-130-01)

Marketing

Marketing Status
Marketed Since 2025-02-15
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": ["INTRAMUSCULAR"], "spl_id": "64ba1614-82e8-476f-957d-a29198c7a26e", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["5831e15a-3efa-48bb-9d49-8451f78d9868"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (65219-130-02)  / 2 mL in 1 VIAL (65219-130-01)", "package_ndc": "65219-130-02", "marketing_start_date": "20250215"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "65219-130_64ba1614-82e8-476f-957d-a29198c7a26e", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "65219-130", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA216724", "marketing_category": "ANDA", "marketing_start_date": "20250215", "listing_expiration_date": "20261231"}