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 TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sumatriptan succinate 100 mg/1

Manufacturer
GlaxoSmithKline LLC

Identifiers & Regulatory

Product NDC 0173-0737
Product ID 0173-0737_21c610c9-8ab7-4bc6-bb14-7d5faa26a0fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020132
Listing Expiration 2026-12-31
Marketing Start 2003-12-19

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 01730737
Hyphenated Format 0173-0737

Supplemental Identifiers

RxCUI
208450 209169 284460 313160 313161 315223
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 NDA020132 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1 CARTON in 1 CARTON (0173-0737-01) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0173-0737-01 1 CARTON in 1 CARTON (0173-0737-01) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

sumatriptan succinate (100 mg/1)

Linked Drug Pages (1)

IMITREX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21c610c9-8ab7-4bc6-bb14-7d5faa26a0fc", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["208450", "209169", "284460", "313160", "313161", "315223"], "spl_set_id": ["584abe73-8290-4484-ff8e-5890831c095e"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CARTON in 1 CARTON (0173-0737-01)  / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0173-0737-01", "marketing_start_date": "20031219"}], "brand_name": "IMITREX", "product_id": "0173-0737_21c610c9-8ab7-4bc6-bb14-7d5faa26a0fc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "0173-0737", "generic_name": "sumatriptan", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IMITREX", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "NDA020132", "marketing_category": "NDA", "marketing_start_date": "20031219", "listing_expiration_date": "20261231"}