methohexital sodium

Generic: methohexital sodium

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methohexital sodium
Generic Name methohexital sodium
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS RECTAL
Active Ingredients

methohexital sodium 500 mg/500mg

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-893
Product ID 23155-893_9ec15df7-278e-4cf3-bc97-e480b4671ca6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215488
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2024-12-12

Pharmacologic Class

Classes
barbiturate [epc] barbiturates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155893
Hyphenated Format 23155-893

Supplemental Identifiers

RxCUI
1244233
UPC
0323155893311 0011100004492
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
INTRAMUSCULAR INTRAVENOUS RECTAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/500mg
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (23155-893-31) / 500 mg in 1 VIAL
source: ndc

Packages (1)

23155-893-31 1 VIAL in 1 CARTON (23155-893-31) / 500 mg in 1 VIAL

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": ["INTRAMUSCULAR", "INTRAVENOUS", "RECTAL"], "spl_id": "9ec15df7-278e-4cf3-bc97-e480b4671ca6", "openfda": {"upc": ["0323155893311", "0011100004492"], "unii": ["60200PNZ7Q"], "rxcui": ["1244233"], "spl_set_id": ["f76d4ab9-2f6c-420b-afec-b9cdfdc083ce"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (23155-893-31)  / 500 mg in 1 VIAL", "package_ndc": "23155-893-31", "marketing_start_date": "20241212"}], "brand_name": "Methohexital Sodium", "product_id": "23155-893_9ec15df7-278e-4cf3-bc97-e480b4671ca6", "dosage_form": "INJECTION", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]"], "product_ndc": "23155-893", "dea_schedule": "CIV", "generic_name": "Methohexital Sodium", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "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": "20241212", "listing_expiration_date": "20261231"}