FDA.reportPublic FDA data

NDC 0009-7807-01 - Zyvox

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
0009-7807
Requested NDC
0009-7807-01
Package NDCs from labels
0009-7807-01, 0009-7807-02
Manufacturer
Pharmacia & Upjohn Company LLC | Pfizer Asia Manufacturing Pte Ltd
Effective date
2026-07-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Zyvox - Pharmacia & Upjohn Company LLC | Pfizer Asia Manufacturing Pte LtdPharmacia & Upjohn Company LLC | Pfizer Asia Manufacturing Pte Ltd2026-07-09HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0009-7807-01Zyvox300 mL in 1 BAGINJECTION, SOLUTION30023
0009-7807-02Zyvox10 in 1 BOXINJECTION, SOLUTION1023

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0009-7807ZYVOX (LINEZOLID) INJECTION, SOLUTION [PHARMACIA & UPJOHN COMPANY LLC]20Current NDC, Legacy NDC, 2 package rows20240927_3e5e9975-6f36-42e4-ab46-0e75dda83592.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0009-7807-01ML - Milliliter0009-7807c5ff3042-7e83-4b46-8339-eab229c6f8cc12015-06-09
0009-7807-02ML - Milliliter0009-7807df08c8f2-4916-4254-bc2f-673bec09e68312015-06-09

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LINEZOLIDACTIVE INGREDIENTISQ9I6J12JZYVOX (LINEZOLID) INJECTION, SOLUTION [PHARMACIA AND UPJOHN COMPANY]3
LINEZOLIDACTIVE MOIETYISQ9I6J12JZYVOX (LINEZOLID) INJECTION, SOLUTION [PHARMACIA AND UPJOHN COMPANY]3
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPZYVOX (LINEZOLID) INJECTION, SOLUTION [PHARMACIA AND UPJOHN COMPANY]3
DEXTROSEINACTIVE INGREDIENTIY9XDZ35W2ZYVOX (LINEZOLID) INJECTION, SOLUTION [PHARMACIA AND UPJOHN COMPANY]3
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULRZYVOX (LINEZOLID) INJECTION, SOLUTION [PHARMACIA AND UPJOHN COMPANY]3

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 2 of 15 · 291 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Infant DextroseDEXTROSEHenry Schein, Inc.ce71d929-d11e-444c-bd45-e025d51720572026-07-13Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
LinezolidLINEZOLIDEugia US LLCb721756c-3b5e-456d-a2f6-0d8a56cc7f352026-07-13Warnings, Adverse reactionsExact identifier
rxcui: 1662285
unii: ISQ9I6J12J
ZyvoxLINEZOLIDPharmacia & Upjohn Company LLC3e5e9975-6f36-42e4-ab46-0e75dda835922026-07-09Warnings, Adverse reactionsExact identifier
application number: NDA021131
ndc (package): 0009-7807-02
ndc (package): 0009-7807-01
ndc (product): 0009-7807
ndc11 (package): 00009780701
rxcui: 1662286
rxcui: 1662285
spl id: 2f3e1cfd-948d-4e75-95c1-11c7cd4be3ef
spl set id: 3e5e9975-6f36-42e4-ab46-0e75dda83592
unii: ISQ9I6J12J
LinezolidLINEZOLIDMylan Pharmaceuticals Inc.83a84897-ccca-42a1-ab1a-bbf1d43a982b2026-07-09Warnings, Adverse reactionsExact identifier
unii: ISQ9I6J12J
LinezolidLINEZOLIDSportpharm LLC7368298b-d75c-4950-bbc1-00fc53f472ec2026-07-02Warnings, Adverse reactionsExact identifier
unii: ISQ9I6J12J
Leukotrap WB SystemCPDA-1 BLOOD BAG COLLECTION SYSTEMGVS TM INC54fd8a72-0527-df0c-e063-6294a90abe752026-06-24Exact identifier
unii: LX22YL083G
Leukotrap WB SystemCPDA-1 BLOOD BAG COLLECTION SYSTEMGVS TM INC54fddca1-b40c-7af0-e063-6294a90a410e2026-06-24Exact identifier
unii: LX22YL083G
Leukotrap WB SystemCPDA-1 BLOOD BAG COLLECTION SYSTEMGVS TM INC54fdf83e-f641-1f69-e063-6394a90ab7502026-06-24Exact identifier
unii: LX22YL083G
DextroseDEXTROSE MONOHYDRATEHospira, Inc.672264e3-9709-4bba-2a9d-12bf70c7396a2026-06-24Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
ZyvoxLINEZOLIDPharmacia & Upjohn Company LLC6e70e63b-bfd5-478d-a8ee-8ba22c9efabd2026-06-23Warnings, Adverse reactionsExact identifier
application number: NDA021131
rxcui: 1662286
rxcui: 1662285
unii: ISQ9I6J12J
LinezolidLINEZOLIDHospira, Inc.c401f1a8-cc37-461b-bfef-f2e156629bf82026-06-19Warnings, Adverse reactionsExact identifier
rxcui: 1662285
unii: ISQ9I6J12J
LinezolidLINEZOLIDSandoz Inca287cdf4-47a8-459f-8890-86181af5e8362026-06-15Warnings, Adverse reactionsExact identifier
rxcui: 1662285
unii: ISQ9I6J12J
E-Z-GAS IIANTACID/ANTIFLATULENTE-Z-EM, INC.4e12e1cb-b033-076d-e054-00144ff8d46c2026-06-15WarningsExact identifier
unii: XF417D3PSL
ACD ACITRIC ACID MONOHYDRATE, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATETerumo BCT, Ltd.395aec48-198a-4aed-8e38-7accfb3232f92026-06-15Warnings, Adverse reactionsExact identifier
unii: B22547B95K
unii: LX22YL083G
BM BM182 DROPSHEPAR SULF, GRAPHITES, MERC SOL, MURIATIC ACIDTotal Operations Management LLC DBA:Bestmade Natural Products Micro5423bde6-3e31-38b0-e063-6294a90afb2d2026-06-13WarningsExact identifier
unii: QTT17582CB
BM BM182 DROPSHEPAR SULF, GRAPHITES, MERC SOL, MURIATIC ACIDBM Private Limited540d11e3-e4a1-0ca2-e063-6394a90a3c262026-06-12WarningsExact identifier
unii: QTT17582CB
LinezolidLINEZOLIDREMEDYREPACK INC.3e0d868d-f419-47e8-a3bc-41ececac468b2026-06-12Warnings, Adverse reactionsExact identifier
unii: ISQ9I6J12J
Sodium Citrate and Citric AcidSODIUM CITRATE AND CITRIC ACID MONOHYDRATECardinal Health 107, LLCb3d5225c-0ee4-481e-b9ec-bc5e1321096d2026-06-12Adverse reactionsExact identifier
unii: XF417D3PSL
DEXTROSEDEXTROSE MONOHYDRATEBaxter Healthcare Corporation3bb406a9-f5cb-403a-b1bb-5c4facbea3d52026-06-11Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
DextroseDEXTROSE MONOHYDRATEHospira, Inc.10e98cb0-31a5-4ad1-3eaa-aa4af387a42d2026-06-02Warnings, Adverse reactionsExact identifier
unii: LX22YL083G

Reported adverse events (FAERS/openFDA)#

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