sumatriptan

Generic: sumatriptan

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sumatriptan succinate 100 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-404
Product ID 72189-404_2c4ce2c4-2b16-de10-e063-6394a90ad371
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078284
Listing Expiration 2026-12-31
Marketing Start 2022-12-13

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 72189404
Hyphenated Format 72189-404

Supplemental Identifiers

RxCUI
313160
UNII
J8BDZ68989

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 sumatriptan (source: ndc)
Generic Name sumatriptan (source: ndc)
Application Number ANDA078284 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 9 TABLET, FILM COATED in 1 BOTTLE (72189-404-09)
source: ndc

Packages (1)

72189-404-09 9 TABLET, FILM COATED in 1 BOTTLE (72189-404-09)

Ingredients (1)

sumatriptan succinate (100 mg/1)

Linked Drug Pages (1)

Sumatriptan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4ce2c4-2b16-de10-e063-6394a90ad371", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160"], "spl_set_id": ["efb7ec4e-0a5d-2aae-e053-2a95a90aebf2"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (72189-404-09)", "package_ndc": "72189-404-09", "marketing_start_date": "20221213"}], "brand_name": "Sumatriptan", "product_id": "72189-404_2c4ce2c4-2b16-de10-e063-6394a90ad371", "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": "72189-404", "generic_name": "Sumatriptan", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078284", "marketing_category": "ANDA", "marketing_start_date": "20221213", "listing_expiration_date": "20261231"}