Package 51662-1406-1

Brand: chlorpromazine hci

Generic: chlorpromazine hci
NDC Package

Package Facts

Identity

Package NDC 51662-1406-1
Digits Only 5166214061
Product NDC 51662-1406
Description

2 mL in 1 AMPULE (51662-1406-1)

Marketing

Marketing Status
Marketed Since 2019-10-21
Brand chlorpromazine hci
Generic chlorpromazine hci
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "2b37c8a2-d5d6-015f-e063-6394a90a3899", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076"], "spl_set_id": ["9575c766-3758-6f33-e053-2995a90ae6b1"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 AMPULE (51662-1406-1)", "package_ndc": "51662-1406-1", "marketing_start_date": "20191021"}], "brand_name": "CHLORPROMAZINE HCI", "product_id": "51662-1406_2b37c8a2-d5d6-015f-e063-6394a90a3899", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51662-1406", "generic_name": "CHLORPROMAZINE HCI", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HCI", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA083329", "marketing_category": "ANDA", "marketing_start_date": "20191021", "listing_expiration_date": "20261231"}