Package 83270-003-01

Brand: methohexital sodium

Generic: methohexital sodium
NDC Package

Package Facts

Identity

Package NDC 83270-003-01
Digits Only 8327000301
Product NDC 83270-003
Product ID 83270-003_4b14107a-95d4-0f90-e063-6394a90a0eb3
Description

500 mg in 1 VIAL (83270-003-01)

Marketing

Marketing Status
Marketed Since 2026-01-24
Brand methohexital sodium
Generic methohexital sodium
Sample Package No

Linked Drug Pages (1)

Methohexital Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "4b14107a-95d4-0f90-e063-6394a90a0eb3", "openfda": {"unii": ["60200PNZ7Q"], "rxcui": ["1244233"], "spl_set_id": ["6fb09acf-4937-47a0-a9da-084ec062da6f"], "manufacturer_name": ["ONESOURCE SPECIALTY PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mg in 1 VIAL (83270-003-01)", "package_ndc": "83270-003-01", "marketing_start_date": "20260124"}], "brand_name": "Methohexital Sodium", "product_id": "83270-003_4b14107a-95d4-0f90-e063-6394a90a0eb3", "dosage_form": "INJECTION", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]"], "product_ndc": "83270-003", "dea_schedule": "CIV", "generic_name": "Methohexital Sodium", "labeler_name": "ONESOURCE SPECIALTY PHARMA LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methohexital Sodium", "active_ingredients": [{"name": "METHOHEXITAL SODIUM", "strength": "500 mg/500mg"}], "application_number": "ANDA215488", "marketing_category": "ANDA", "marketing_start_date": "20260124", "listing_expiration_date": "20271231"}