imitrex

Generic: sumatriptan

Labeler: glaxosmithkline llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name imitrex
Generic Name sumatriptan
Labeler glaxosmithkline llc
Dosage Form INJECTION
Routes
SUBCUTANEOUS
Active Ingredients

sumatriptan succinate 4 mg/.5mL

Manufacturer
GlaxoSmithKline LLC

Identifiers & Regulatory

Product NDC 0173-0739
Product ID 0173-0739_f5834e77-047f-43ab-8b9c-37d3b34afc27
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020080
Listing Expiration 2026-12-31
Marketing Start 2006-04-06

Pharmacologic Class

Classes
serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa] serotonin-1b and serotonin-1d receptor agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01730739
Hyphenated Format 0173-0739

Supplemental Identifiers

RxCUI
758523 860088 1657160 1657173
UNII
J8BDZ68989

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 imitrex (source: ndc)
Generic Name sumatriptan (source: ndc)
Application Number NDA020080 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 4 mg/.5mL
source: ndc
Packaging
  • 2 SYRINGE in 1 PACKAGE (0173-0739-00) / .5 mL in 1 SYRINGE
  • 2 SYRINGE in 1 CARTON (0173-0739-02) / .5 mL in 1 SYRINGE
source: ndc

Packages (2)

Ingredients (1)

sumatriptan succinate (4 mg/.5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "f5834e77-047f-43ab-8b9c-37d3b34afc27", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["758523", "860088", "1657160", "1657173"], "spl_set_id": ["fee7d073-0b99-48f2-7985-0d8cf970894b"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 SYRINGE in 1 PACKAGE (0173-0739-00)  / .5 mL in 1 SYRINGE", "package_ndc": "0173-0739-00", "marketing_start_date": "20060406"}, {"sample": false, "description": "2 SYRINGE in 1 CARTON (0173-0739-02)  / .5 mL in 1 SYRINGE", "package_ndc": "0173-0739-02", "marketing_start_date": "20060406"}], "brand_name": "IMITREX", "product_id": "0173-0739_f5834e77-047f-43ab-8b9c-37d3b34afc27", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "0173-0739", "generic_name": "sumatriptan", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IMITREX", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "4 mg/.5mL"}], "application_number": "NDA020080", "marketing_category": "NDA", "marketing_start_date": "20060406", "listing_expiration_date": "20261231"}