sumatriptan

Generic: sumatriptan

Labeler: florida pharmaceutical products, llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan
Labeler florida pharmaceutical products, llc.
Dosage Form SPRAY
Routes
NASAL
Active Ingredients

sumatriptan 20 mg/1

Manufacturer
Florida Pharmaceutical Products, LLC.

Identifiers & Regulatory

Product NDC 71921-170
Product ID 71921-170_d0b56323-49ef-f239-e053-2a95a90ae766
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208967
Listing Expiration 2026-12-31
Marketing Start 2021-05-15

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 71921170
Hyphenated Format 71921-170

Supplemental Identifiers

RxCUI
314227
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 ANDA208967 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 6 CONTAINER in 1 BOX (71921-170-61) / 1 SPRAY in 1 CONTAINER
source: ndc

Packages (1)

71921-170-61 6 CONTAINER in 1 BOX (71921-170-61) / 1 SPRAY in 1 CONTAINER

Ingredients (1)

sumatriptan (20 mg/1)

Linked Drug Pages (1)

Sumatriptan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "d0b56323-49ef-f239-e053-2a95a90ae766", "openfda": {"nui": ["N0000175763", "N0000175764", "N0000175765"], "unii": ["8R78F6L9VO"], "rxcui": ["314227"], "spl_set_id": ["267dadc1-6960-4d8b-88ef-86be9c5f7159"], "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": ["Florida Pharmaceutical Products, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 CONTAINER in 1 BOX (71921-170-61)  / 1 SPRAY in 1 CONTAINER", "package_ndc": "71921-170-61", "marketing_start_date": "20210515"}], "brand_name": "Sumatriptan", "product_id": "71921-170_d0b56323-49ef-f239-e053-2a95a90ae766", "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": "71921-170", "generic_name": "sumatriptan", "labeler_name": "Florida Pharmaceutical Products, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN", "strength": "20 mg/1"}], "application_number": "ANDA208967", "marketing_category": "ANDA", "marketing_start_date": "20210515", "listing_expiration_date": "20261231"}