United States · FDA National Drug Code directory
GEMTESA
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 73336-075_6744a1cf-7abb-4623-85e3-8f67a9eb19d4
- Product NDC
- 73336-075
- Form
- TABLET, FILM COATED
- Composition / generic term
- vibegron
- Labeler
- Sumitomo Pharma America, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20201229
- Source listing expiry
- 20261231
Source-listed ingredients
- VIBEGRON — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (73336-075-07) / 7 TABLET, FILM COATED in 1 BOTTLE · 73336-075-07
- 30 TABLET, FILM COATED in 1 BOTTLE (73336-075-30) · 73336-075-30
- 90 TABLET, FILM COATED in 1 BOTTLE (73336-075-90) · 73336-075-90
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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