sumatriptan
Generic: sumatriptan
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
sumatriptan
Generic Name
sumatriptan
Labeler
a-s medication solutions
Dosage Form
INJECTION
Routes
Active Ingredients
sumatriptan succinate 6 mg/.5mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-2497
Product ID
50090-2497_32d8434e-550e-4ba9-a709-eb10fe9a596f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200183
Listing Expiration
2026-12-31
Marketing Start
2013-09-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500902497
Hyphenated Format
50090-2497
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 (source: ndc)
Application Number
ANDA200183 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 mg/.5mL
Packaging
- 5 VIAL in 1 CARTON (50090-2497-0) / .5 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "32d8434e-550e-4ba9-a709-eb10fe9a596f", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313165"], "spl_set_id": ["f675d0db-f356-4eda-be62-b00af476326c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (50090-2497-0) / .5 mL in 1 VIAL", "package_ndc": "50090-2497-0", "marketing_start_date": "20161013"}], "brand_name": "SUMATRIPTAN", "product_id": "50090-2497_32d8434e-550e-4ba9-a709-eb10fe9a596f", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "50090-2497", "generic_name": "sumatriptan", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUMATRIPTAN", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "6 mg/.5mL"}], "application_number": "ANDA200183", "marketing_category": "ANDA", "marketing_start_date": "20130916", "listing_expiration_date": "20261231"}