NDC 70121-1685 – Exenatide

Exenatide 250 ug/mL · Injection · Subcutaneous

Human Prescription Drug

Product NDC70121-1685

Product details

Brand name
Exenatide
Generic name
Exenatide
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Injection
Route
Subcutaneous
Marketing category
ANDA · ANDA206697
Marketed since
November 22, 2024
Marketing end
June 30, 2027
Pharmacologic class
GLP-1 Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Exenatide →

Package NDC codes (1)

Package NDCDescriptionSince
70121-1685-11 CARTRIDGE in 1 CARTON (70121-1685-1) / 1.2 mL in 1 CARTRIDGENov 22, 2024

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