sumatriptan succinate
Generic: sumatriptan succinate
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
sumatriptan succinate
Generic Name
sumatriptan succinate
Labeler
asclemed usa, inc.
Dosage Form
TABLET
Routes
Active Ingredients
sumatriptan succinate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76420-093
Product ID
76420-093_b26ec84b-1af1-b04d-e053-2a95a90a8c78
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076847
Listing Expiration
2026-12-31
Marketing Start
2009-11-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420093
Hyphenated Format
76420-093
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 succinate (source: ndc)
Generic Name
sumatriptan succinate (source: ndc)
Application Number
ANDA076847 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 9 BLISTER PACK in 1 CARTON (76420-093-09) / 1 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": "b26ec84b-1af1-b04d-e053-2a95a90a8c78", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313161"], "spl_set_id": ["b16886d0-224b-4d83-85c4-bc3eb3606c17"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 BLISTER PACK in 1 CARTON (76420-093-09) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "76420-093-09", "marketing_start_date": "20201024"}], "brand_name": "Sumatriptan Succinate", "product_id": "76420-093_b26ec84b-1af1-b04d-e053-2a95a90a8c78", "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": "76420-093", "generic_name": "Sumatriptan Succinate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA076847", "marketing_category": "ANDA", "marketing_start_date": "20091117", "listing_expiration_date": "20261231"}