methohexital sodium

Generic: methohexital sodium

Labeler: onesource specialty pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methohexital sodium
Generic Name methohexital sodium
Labeler onesource specialty pharma limited
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

methohexital sodium 500 mg/500mg

Manufacturer
ONESOURCE SPECIALTY PHARMA LIMITED

Identifiers & Regulatory

Product NDC 83270-003
Product ID 83270-003_4b14107a-95d4-0f90-e063-6394a90a0eb3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215488
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 2026-01-24

Pharmacologic Class

Classes
barbiturate [epc] barbiturates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83270003
Hyphenated Format 83270-003

Supplemental Identifiers

RxCUI
1244233
UNII
60200PNZ7Q

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methohexital sodium (source: ndc)
Generic Name methohexital sodium (source: ndc)
Application Number ANDA215488 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/500mg
source: ndc
Packaging
  • 500 mg in 1 VIAL (83270-003-01)
source: ndc

Packages (1)

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

Ingredients (1)

methohexital sodium (500 mg/500mg)

Linked Drug Pages (1)

Methohexital Sodium ndc-match (0.9)

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"}