sumatriptan

Generic: sumatriptan

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sumatriptan succinate 100 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8535
Product ID 68788-8535_4f1c703b-25a8-4b6d-953f-3782ff39b585
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078284
Listing Expiration 2026-12-31
Marketing Start 2023-10-23

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 687888535
Hyphenated Format 68788-8535

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 BLISTER PACK (68788-8535-9)
source: ndc

Packages (1)

68788-8535-9 9 TABLET, FILM COATED in 1 BLISTER PACK (68788-8535-9)

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": "4f1c703b-25a8-4b6d-953f-3782ff39b585", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160"], "spl_set_id": ["ff08b9ee-03bf-4f5b-930e-233a3b8866af"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BLISTER PACK (68788-8535-9)", "package_ndc": "68788-8535-9", "marketing_start_date": "20231023"}], "brand_name": "Sumatriptan", "product_id": "68788-8535_4f1c703b-25a8-4b6d-953f-3782ff39b585", "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": "68788-8535", "generic_name": "Sumatriptan", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20231023", "listing_expiration_date": "20261231"}