WEGOVY

Product NDC
0169-1624
11-digit product format
001691624
Labeler code
0169
Product ID
0169-1624_2cf550fd-3019-4202-b112-2009de398600
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
semaglutide
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Labeler
Novo Nordisk Pharmaceutical Industries, LP
Application
NDA215256
Marketing category
NDA
Marketing start
2021-06-05
Substance
SEMAGLUTIDE
Active strength
3.2 mg/mL
Pharmacologic classes
GLP-1 Receptor Agonist [EPC], Glucagon-Like Peptide 1 [CS], Glucagon-like Peptide-1 (GLP-1) Agonists [MoA]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
53AXN4NNHXSEMAGLUTIDE910463-68-2SEMAGLUTIDE

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
WEGOVYNovo Nordisk Pharmaceutical Industries, LP2026-05-05HUMAN PRESCRIPTION DRUG LABEL18
WEGOVYNovo Nordisk2025-08-01HUMAN PRESCRIPTION DRUG LABEL11