sumatriptan

Generic: sumatriptan succinate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan succinate
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sumatriptan succinate 100 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1184
Product ID 70518-1184_48c05e3e-936b-7f12-e063-6294a90a2c4e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078327
Listing Expiration 2027-12-31
Marketing Start 2018-05-14

Pharmacologic Class

Classes
serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa] serotonin-1b and serotonin-1d receptor agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181184
Hyphenated Format 70518-1184

Supplemental Identifiers

RxCUI
313160
UNII
J8BDZ68989

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (70518-1184-0) / 9 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

sumatriptan succinate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c05e3e-936b-7f12-e063-6294a90a2c4e", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160"], "spl_set_id": ["73c9ac06-b55e-41e0-90ec-deb250f37eb5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (70518-1184-0)  / 9 TABLET in 1 BLISTER PACK", "package_ndc": "70518-1184-0", "marketing_start_date": "20180514"}], "brand_name": "Sumatriptan", "product_id": "70518-1184_48c05e3e-936b-7f12-e063-6294a90a2c4e", "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": "70518-1184", "generic_name": "Sumatriptan Succinate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078327", "marketing_category": "ANDA", "marketing_start_date": "20180514", "listing_expiration_date": "20271231"}