sumatriptan

Generic: sumatriptan

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan
Labeler lannett company, inc.
Dosage Form SPRAY
Routes
NASAL
Active Ingredients

sumatriptan 20 mg/.1mL

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-1859
Product ID 0527-1859_1fca524e-6cf5-4782-b5d5-b37b101cd93a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204841
Listing Expiration 2026-12-31
Marketing Start 2016-02-19

Pharmacologic Class

Established (EPC)
serotonin-1b and serotonin-1d receptor agonist [epc]
Mechanism of Action
serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05271859
Hyphenated Format 0527-1859

Supplemental Identifiers

RxCUI
313159 314227
UPC
0305271818430 0305271859433
UNII
8R78F6L9VO
NUI
N0000175763 N0000175764 N0000175765

Packaging Origin

Original Packager
true

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 ANDA204841 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/.1mL
source: ndc
Packaging
  • 6 BLISTER PACK in 1 CARTON (0527-1859-43) / .1 mL in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

sumatriptan (20 mg/.1mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "1fca524e-6cf5-4782-b5d5-b37b101cd93a", "openfda": {"nui": ["N0000175763", "N0000175764", "N0000175765"], "upc": ["0305271818430", "0305271859433"], "unii": ["8R78F6L9VO"], "rxcui": ["313159", "314227"], "spl_set_id": ["64efe12a-cc43-47e6-b3dc-21dab6ddae06"], "pharm_class_epc": ["Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "pharm_class_moa": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (0527-1859-43)  / .1 mL in 1 BLISTER PACK", "package_ndc": "0527-1859-43", "marketing_start_date": "20160219"}], "brand_name": "Sumatriptan", "product_id": "0527-1859_1fca524e-6cf5-4782-b5d5-b37b101cd93a", "dosage_form": "SPRAY", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "0527-1859", "generic_name": "Sumatriptan", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN", "strength": "20 mg/.1mL"}], "application_number": "ANDA204841", "marketing_category": "ANDA", "marketing_start_date": "20160219", "listing_expiration_date": "20261231"}