NDC 0310-6512 – Byetta

Exenatide 250 ug/mL · Injection · Subcutaneous

Human Prescription Drug

Product NDC0310-6512

Product details

Brand name
Byetta
Generic name
Exenatide
Labeler
AstraZeneca Pharmaceuticals LP
Dosage form
Injection
Route
Subcutaneous
Marketing category
NDA · NDA021773
Marketed since
December 10, 2014
Marketing end
December 31, 2026
Pharmacologic class
GLP-1 Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Byetta →

Package NDC codes (1)

Package NDCDescriptionSince
0310-6512-011 CARTRIDGE in 1 CARTON (0310-6512-01) / 1.2 mL in 1 CARTRIDGEDec 10, 2014

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