sevoflurane

Generic: sevoflurane

Labeler: halocarbon life sciences, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sevoflurane
Generic Name sevoflurane
Labeler halocarbon life sciences, llc
Dosage Form LIQUID
Routes
RESPIRATORY (INHALATION)
Active Ingredients

sevoflurane 1 mL/mL

Manufacturer
Halocarbon Life Sciences, LLC

Identifiers & Regulatory

Product NDC 12164-005
Product ID 12164-005_2409685f-f867-4b3d-bc58-6bd2749bbb2a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078650
Listing Expiration 2026-12-31
Marketing Start 2007-11-19

Pharmacologic Class

Established (EPC)
general anesthetic [epc]
Physiologic Effect
general anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 12164005
Hyphenated Format 12164-005

Supplemental Identifiers

RxCUI
200243
UNII
38LVP0K73A
NUI
N0000175975 N0000175681

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 sevoflurane (source: ndc)
Generic Name sevoflurane (source: ndc)
Application Number ANDA078650 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 1 mL/mL
source: ndc
Packaging
  • 250 mL in 1 BOTTLE (12164-005-25)
source: ndc

Packages (1)

Ingredients (1)

sevoflurane (1 mL/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "2409685f-f867-4b3d-bc58-6bd2749bbb2a", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["38LVP0K73A"], "rxcui": ["200243"], "spl_set_id": ["bdde7502-6218-401c-9a4f-dd3bc3a80f72"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Halocarbon Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BOTTLE (12164-005-25)", "package_ndc": "12164-005-25", "marketing_start_date": "20071119"}], "brand_name": "Sevoflurane", "product_id": "12164-005_2409685f-f867-4b3d-bc58-6bd2749bbb2a", "dosage_form": "LIQUID", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "12164-005", "generic_name": "sevoflurane", "labeler_name": "Halocarbon Life Sciences, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sevoflurane", "active_ingredients": [{"name": "SEVOFLURANE", "strength": "1 mL/mL"}], "application_number": "ANDA078650", "marketing_category": "ANDA", "marketing_start_date": "20071119", "listing_expiration_date": "20261231"}