NDC 0169-1715 – Ozempic

Semaglutide 1.5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0169-1715

Product details

Brand name
Ozempic
Generic name
Oral semaglutide
Labeler
Novo Nordisk Pharmaceutical Industries, LP
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA213051
Marketed since
April 27, 2026
Listing expires
December 31, 2027
Pharmacologic class
GLP-1 Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ozempic →

Package NDC codes (2)

Package NDCDescriptionSince
0169-1715-3030 TABLET in 1 BOTTLE, PLASTIC (0169-1715-30)Apr 27, 2026
0169-1715-90 sample30 TABLET in 1 BOTTLE, PLASTIC (0169-1715-90)Apr 27, 2026

Recalls mentioning this NDC

Other Ozempic products