sumatriptan

Generic: sumatriptan succinate

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

Drug Facts

Product Profile

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

sumatriptan succinate 25 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-6769
Product ID 68788-6769_d44ab3f6-b246-479c-906b-eb94f6549a1c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078327
Listing Expiration 2026-12-31
Marketing Start 2016-10-24

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 687886769
Hyphenated Format 68788-6769

Supplemental Identifiers

RxCUI
315223
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 succinate (source: ndc)
Application Number ANDA078327 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 9 TABLET in 1 BLISTER PACK (68788-6769-9)
source: ndc

Packages (1)

68788-6769-9 9 TABLET in 1 BLISTER PACK (68788-6769-9)

Ingredients (1)

sumatriptan succinate (25 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": "d44ab3f6-b246-479c-906b-eb94f6549a1c", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["315223"], "spl_set_id": ["baf37e8c-d414-4ca7-a366-97dc202372ff"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BLISTER PACK (68788-6769-9)", "package_ndc": "68788-6769-9", "marketing_start_date": "20161024"}], "brand_name": "Sumatriptan", "product_id": "68788-6769_d44ab3f6-b246-479c-906b-eb94f6549a1c", "dosage_form": "TABLET", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "68788-6769", "generic_name": "Sumatriptan Succinate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA078327", "marketing_category": "ANDA", "marketing_start_date": "20161024", "listing_expiration_date": "20261231"}