sumatriptan
Generic: sumatriptan succinate
Labeler: preferred pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
sumatriptan
Generic Name
sumatriptan succinate
Labeler
preferred pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
sumatriptan succinate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-6778
Product ID
68788-6778_9c1d3c4c-d129-4c1f-83c4-0758ccb26182
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078327
Listing Expiration
2026-12-31
Marketing Start
2016-10-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687886778
Hyphenated Format
68788-6778
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (68788-6778-9) / 9 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9c1d3c4c-d129-4c1f-83c4-0758ccb26182", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160"], "spl_set_id": ["bf9fd9fe-095b-4478-bd2e-a5534af07761"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68788-6778-9) / 9 TABLET in 1 BLISTER PACK", "package_ndc": "68788-6778-9", "marketing_start_date": "20161024"}], "brand_name": "Sumatriptan", "product_id": "68788-6778_9c1d3c4c-d129-4c1f-83c4-0758ccb26182", "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": "68788-6778", "generic_name": "Sumatriptan Succinate", "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": "ANDA078327", "marketing_category": "ANDA", "marketing_start_date": "20161024", "listing_expiration_date": "20261231"}