Identity recordProduct-specific FDA and EU medicine records
What Liraglutide resolves to
SAXENDA is a product-specific liraglutide prescription medicine authorized in the United States and European Union for defined populations and uses. Those authorizations do not transfer to every liraglutide product, compounded preparation, imported pen, indication, presentation, online seller, or supply route, and they do not establish current launch, reimbursement, availability, or authorization outside those records.
- Evidence lane
- FDA-approved medicine
- Current record
- NDA 206321 · FDA-approved prescription drug
- Checked
- July 17, 2026
liraglutideSaxendaNN2211NDA 206321GLP-1 receptor agonist
Destination recordPemeriksaan produk BPOM dan distribusi wajib
What Indonesia still has to prove
Panduan Indonesia untuk mencocokkan klaim produk terkait peptida di Cek BPOM dan memeriksa bukti distribusi farmasi yang tersertifikasi, masih berlaku, atau telah dicabut melalui catatan CDOB publik sebelum menilai penjual, produk impor, pasar daring, bahan riset, atau jalur pasok.
- Comparison mode
- Rupiah / catatan produk BPOM dan distribusi CDOB
- Price coverage
- Belum ada tabel penjual Indonesia yang memenuhi syarat
- Guide updated
- 18 Juli 2026