FDA.reportPublic FDA data

NDC 0169-4303-90 - OZEMPIC

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0169-4303
Requested NDC
0169-4303-90
Package NDCs from labels
0169-4303-01, 0169-4303-13, 0169-4303-90, 0169-4303-93, 0169-4303-30, 0169-4303-99
Manufacturer
Novo Nordisk Pharmaceutical Industries, LP
Effective date
2026-01-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
OZEMPIC - Novo Nordisk Pharmaceutical Industries, LPNovo Nordisk Pharmaceutical Industries, LP2026-01-30HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0169-4303-01RYBELSUS10 in 1 BLISTER PACKTABLET1013
0169-4303-13RYBELSUS3 in 1 CARTONTABLET313
0169-4303-30RYBELSUS30 in 1 BOTTLE, GLASSTABLET3013
0169-4303-90RYBELSUS10 in 1 BLISTER PACKTABLET1013
0169-4303-93RYBELSUS3 in 1 CARTONTABLET313
0169-4303-99RYBELSUS30 in 1 BOTTLE, GLASSTABLET3013

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0169-4303RYBELSUS (ORAL SEMAGLUTIDE) TABLET [NOVO NORDISK]10Current NDC, Legacy NDC, 6 package rows20241225_27f15fac-7d98-4114-a2ec-92494a91da98.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0169-4303-13EA - Each0169-4303f71e0dbf-c777-4687-b17f-065f74cbdda912019-10-07
0169-4303-30EA - Each0169-4303b3fb4eab-087f-4957-b021-92202d1b092012021-11-09
0169-4303-99EA - Each0169-43032572e65f-5d6d-4d29-a919-f2a953b13e9412023-05-05

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 6 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OzempicSEMAGLUTIDEA-S Medication Solutions42bdd912-2393-44c4-b7e0-47672ca289912026-07-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 53AXN4NNHX
OZEMPICORAL SEMAGLUTIDENovo Nordisk Pharmaceutical Industries, LP27f15fac-7d98-4114-a2ec-92494a91da982026-01-30Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA213051
ndc (package): 0169-4307-13
ndc (package): 0169-4303-13
ndc (package): 0169-4815-90
ndc (package): 0169-4314-01
ndc (package): 0169-4314-30
ndc (package): 0169-4303-93
ndc (package): 0169-4815-30
ndc (package): 0169-4307-30
ndc (package): 0169-4303-30
ndc (package): 0169-4314-13
ndc (package): 0169-1704-30
ndc (package): 0169-1715-30
ndc (package): 0169-4809-30
ndc (package): 0169-1715-90
ndc (package): 0169-4303-99
ndc (package): 0169-4303-90
ndc (package): 0169-4303-01
ndc (package): 0169-4307-01
ndc (package): 0169-1709-30
ndc (package): 0169-4804-30
ndc (product): 0169-4809
ndc (product): 0169-1715
ndc (product): 0169-4303
ndc (product): 0169-4804
ndc (product): 0169-4815
ndc (product): 0169-4314
ndc (product): 0169-4307
ndc (product): 0169-1709
ndc (product): 0169-1704
ndc11 (package): 00169430390
rxcui: 2200652
rxcui: 2707553
rxcui: 2707549
rxcui: 2707557
rxcui: 2200658
rxcui: 2200654
rxcui: 2200650
rxcui: 2200644
rxcui: 2736944
rxcui: 2707551
rxcui: 2736946
rxcui: 2736948
rxcui: 2707555
rxcui: 2707547
rxcui: 2200656
spl id: 6834044a-22f1-4f35-b846-b3448ee84c16
spl set id: 27f15fac-7d98-4114-a2ec-92494a91da98
unii: 53AXN4NNHX
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
WEGOVYSEMAGLUTIDEA-S Medication Solutionsf5e548d0-cc79-4c34-a3f5-e20a5b8b65642024-04-23Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 53AXN4NNHX
OzempicSEMAGLUTIDEA-S Medication Solutions979e4df4-0597-48ea-b51c-0f699fa6d1662023-11-22Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 53AXN4NNHX
OZEMPICSEMAGLUTIDEA-S Medication Solutionse6da837c-0da0-41d6-973c-5559bf7643672023-11-17Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 53AXN4NNHX

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.