brevital sodium

Generic: methohexital sodium

Labeler: par health usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name brevital sodium
Generic Name methohexital sodium
Labeler par health usa, llc
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS RECTAL
Active Ingredients

methohexital sodium 500 mg/1

Manufacturer
Par Health USA, LLC

Identifiers & Regulatory

Product NDC 42023-105
Product ID 42023-105_f6691007-12ee-47b7-b487-8bdcbf9e29cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA011559
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2007-11-01

Pharmacologic Class

Classes
barbiturate [epc] barbiturates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42023105
Hyphenated Format 42023-105

Supplemental Identifiers

RxCUI
1244233 1244638
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 brevital sodium (source: ndc)
Generic Name methohexital sodium (source: ndc)
Application Number NDA011559 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS RECTAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (42023-105-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

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

Ingredients (1)

methohexital sodium (500 mg/1)

Linked Drug Pages (1)

Brevital Sodium ndc-match (0.9)

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"}