sumatriptan
Generic: sumatriptan succinate
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
sumatriptan
Generic Name
sumatriptan succinate
Labeler
northstar rx llc
Dosage Form
TABLET
Routes
Active Ingredients
sumatriptan succinate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16714-797
Product ID
16714-797_42e7fb08-6b84-40c3-a59e-0103aedff9be
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078327
Listing Expiration
2026-12-31
Marketing Start
2018-06-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16714797
Hyphenated Format
16714-797
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
- 50 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (16714-797-01) / 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": "42e7fb08-6b84-40c3-a59e-0103aedff9be", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160", "313161", "315223"], "spl_set_id": ["84bfc4ba-4172-4adb-b963-4e0eb438c07a"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (16714-797-01) / 9 TABLET in 1 BLISTER PACK", "package_ndc": "16714-797-01", "marketing_start_date": "20180618"}], "brand_name": "Sumatriptan", "product_id": "16714-797_42e7fb08-6b84-40c3-a59e-0103aedff9be", "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": "16714-797", "generic_name": "Sumatriptan Succinate", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA078327", "marketing_category": "ANDA", "marketing_start_date": "20180618", "listing_expiration_date": "20261231"}