United States · FDA National Drug Code directory
Exenatide
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
- 70121-1685_2141c3ca-074a-4098-85da-1ef78ec4d4dc
- Product NDC
- 70121-1685
- Form
- INJECTION
- Composition / generic term
- Exenatide
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241122 / 20270630
Source-listed ingredients
- EXENATIDE — 250 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 CARTRIDGE in 1 CARTON (70121-1685-1) / 1.2 mL in 1 CARTRIDGE · 70121-1685-1
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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