Package 42023-105-01

Brand: brevital sodium

Generic: methohexital sodium
NDC Package

Package Facts

Identity

Package NDC 42023-105-01
Digits Only 4202310501
Product NDC 42023-105
Product ID 42023-105_f6691007-12ee-47b7-b487-8bdcbf9e29cb
Description

1 VIAL in 1 CARTON (42023-105-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2007-11-01
Brand brevital sodium
Generic methohexital sodium
Sample Package No

Linked Drug Pages (1)

Brevital Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "RECTAL"], "spl_id": "f6691007-12ee-47b7-b487-8bdcbf9e29cb", "openfda": {"unii": ["60200PNZ7Q"], "rxcui": ["1244233", "1244638"], "spl_set_id": ["eccd8340-ead3-4363-8902-0c19d33aa2ac"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (42023-105-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "42023-105-01", "marketing_start_date": "20071101"}], "brand_name": "Brevital Sodium", "product_id": "42023-105_f6691007-12ee-47b7-b487-8bdcbf9e29cb", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]"], "product_ndc": "42023-105", "dea_schedule": "CIV", "generic_name": "methohexital sodium", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Brevital Sodium", "active_ingredients": [{"name": "METHOHEXITAL SODIUM", "strength": "500 mg/1"}], "application_number": "NDA011559", "marketing_category": "NDA", "marketing_start_date": "20071101", "listing_expiration_date": "20261231"}