sumansetron
Generic: sumatriptan succinate, ondansetron
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
sumansetron
Generic Name
sumatriptan succinate, ondansetron
Labeler
puretek corporation
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
59088-772
Product ID
59088-772_f2054b5e-a881-1bd5-e053-2a95a90a015c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2021-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59088772
Hyphenated Format
59088-772
Supplemental Identifiers
RxCUI
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
sumansetron (source: ndc)
Generic Name
sumatriptan succinate, ondansetron (source: ndc)
Resolved Composition
Strengths
- 100 mg
- 25 mg
- 05 unit
- 09 unit
- 50 mg
- 4 mg
- 8 mg
Packaging
- 1 KIT in 1 PACKAGE (59088-772-00) * 9 BLISTER PACK in 1 CARTON (55111-292-09) / 9 TABLET in 1 BLISTER PACK * 30 TABLET, FILM COATED in 1 BOTTLE (45963-538-30)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "f2054b5e-a881-1bd5-e053-2a95a90a015c", "openfda": {"rxcui": ["198052", "313161"], "spl_set_id": ["b69f0762-a2f7-28c7-e053-2995a90a0484"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (59088-772-00) * 9 BLISTER PACK in 1 CARTON (55111-292-09) / 9 TABLET in 1 BLISTER PACK * 30 TABLET, FILM COATED in 1 BOTTLE (45963-538-30)", "package_ndc": "59088-772-00", "marketing_start_date": "20210101"}], "brand_name": "Sumansetron", "product_id": "59088-772_f2054b5e-a881-1bd5-e053-2a95a90a015c", "dosage_form": "KIT", "product_ndc": "59088-772", "generic_name": "sumatriptan succinate, ondansetron", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumansetron", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210101", "listing_expiration_date": "20261231"}