FDA.reportPublic FDA data

NDC 63323-660-01 - Metoprolol

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
63323-660
Requested NDC
63323-660-01
Package NDCs from labels
63323-660-01, 63323-660-05
Manufacturer
Fresenius Kabi USA, LLC
Effective date
2025-09-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Metoprolol - Fresenius Kabi USA, LLCFresenius Kabi USA, LLC2025-09-12HUMAN PRESCRIPTION DRUG LABEL
METOPROLOL TARTRATE - HF Acquisition Co LLC, DBA HealthFirstHF Acquisition Co LLC, DBA HealthFirst2022-12-10HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63323-660-01Metoprolol5 mL in 1 VIALINJECTION, SOLUTION56
63323-660-05Metoprolol10 in 1 TRAYINJECTION, SOLUTION106

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63323-660METOPROLOL (METOPROLOL TARTRATE) INJECTION, SOLUTION [FRESENIUS KABI USA, LLC ]5Current NDC, Legacy NDC, 2 package rows20211117_be1c686e-37a5-4a53-945b-68a6ead35134.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63323-660-01ML - Milliliter63323-6601f8deab4-2d36-43ca-af59-c0b93dc8d86112025-05-14
63323-660-05ML - Milliliter63323-6603fb54e13-15b4-41e1-8a65-22ab42f1b05012012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
METOPROLOL TARTRATEACTIVE INGREDIENTW5S57Y3A5LMETOPROLOL (METOPROLOL TARTRATE) INJECTION, SOLUTION [FRESENIUS KABI USA, LLC]3
METOPROLOLACTIVE MOIETYGEB06NHM23METOPROLOL (METOPROLOL TARTRATE) INJECTION, SOLUTION [FRESENIUS KABI USA, LLC]3
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XMETOPROLOL (METOPROLOL TARTRATE) INJECTION, SOLUTION [FRESENIUS KABI USA, LLC]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 7 of 61 · 1,202 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
METOPROLOL TARTRATEMETOPROLOL TARTRATEREMEDYREPACK INC.5987a15b-e86f-4fd7-a377-35a917c0e3fe2026-06-05Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
Metoprolol TartrateMETOPROLOL TARTRATEDirect_Rx5371c1af-93fa-39db-e063-6394a90a61112026-06-04Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
BM Nat Mur Icing SugarNATRUM MURIATICUM ICING SUGARTotal Operations Management LLC DBA:Bestmade Natural Products Micro5356d350-1325-7299-e063-6294a90a96a02026-06-03WarningsExact identifier
unii: 451W47IQ8X
METOPROLOL TARTRATEMETOPROLOL TARTRATESt. Mary's Medical Park Pharmacye55cd5b5-c739-24ba-e053-2995a90a3ed42026-06-01Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
PlegisolPOTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, AND MAGNESIUM CHLORIDEHospira, Inc.35a174f0-f0d7-4ec7-3f81-d3d572c059cf2026-05-27Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
TPN ElectrolytesSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, AND SODIUM ACETATE ANHYDROUSHospira, Inc.c00817bc-7b62-4abe-0280-e7930eda3f942026-05-25Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Bacteriostatic WaterBACTERIOSTATIC WATERHospira, Inc.87d6e9dc-fe3b-4593-ac9a-d7493d1959c72026-05-22Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Metoprolol TartrateMETOPROLOL TARTRATEHospira, Inc.7c1f998a-233d-4feb-6ea2-457702abd0d22026-05-21Warnings, Adverse reactionsExact identifier
rxcui: 866508
unii: W5S57Y3A5L
SALINE CLEANINGSODIUM CHLORIDEGuangzhou Huanmei Cosmetics Co., Ltd.524f07cc-ddb9-dda5-e063-6394a90ac0a52026-05-21WarningsExact identifier
unii: 451W47IQ8X
Metoprolol TartrateMETOPROLOL TARTRATEPD-Rx Pharmaceuticals, Inc.ab44f4c5-9497-4c92-8545-e4718ddb8f082026-05-21Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
WHITENING SUNSCREENANTI WRINKLEWHITENING SUNSCREENANTI WRINKLEShantou Oushiya Biotechnology Co.,Ltd524384e9-b3f8-4c13-e063-6394a90a89732026-05-20WarningsExact identifier
unii: 059QF0KO0R
METOPROLOL TARTRATEMETOPROLOL TARTRATEREMEDYREPACK INC.f7a05d74-f5e9-4236-a967-c57942a2bbf32026-05-20Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
Sodium ChlorideSODIUM CHLORIDEHospira, Inc.a2a964f7-c3ec-4dfb-e3a0-6d8136a803972026-05-19Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
METOPROLOL TARTRATEMETOPROLOL TARTRATEAphena Pharma Solutions - Tennessee, LLC522c3807-855e-20a3-e063-6394a90abeb72026-05-19Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
METOPROLOL TARTRATEMETOPROLOL TARTRATEAphena Pharma Solutions - Tennessee, LLC522cc739-1252-4689-e063-6294a90ad1b02026-05-19Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
METOPROLOL TARTRATEMETOPROLOL TARTRATEA-S Medication Solutionsef6a817b-58c5-45bc-b5a2-22c31b05c0ab2026-05-19Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
METOPROLOL TARTRATEMETOPROLOL TARTRATEA-S Medication Solutions2bcfb9d9-e092-4a0a-ac55-bad532de360c2026-05-19Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
METOPROLOL TARTRATEMETOPROLOL TARTRATEASCLEMED USA INC.df3492c3-b71a-40d8-838b-031ebca969d82026-05-18Warnings, Adverse reactionsExact identifier
unii: W5S57Y3A5L
HerplexANATHERUM MURICATUM, CLEMATIS ERECTA, MEZEREUM, PHYTOLACCA DECANDRA, RANUNCULUS BULBOSUS, RHUS TOX, THUJA OCCIDENTALIS, NATRUM MURIATICUM, SEPIANashco Products LLCe5e7aa2f-3697-4747-9045-670ea2b135572026-05-14WarningsExact identifier
unii: 451W47IQ8X
NebuClear MDSALINEBlue Echo Care LLC3f85fe62-230f-b0f1-e063-6394a90a5cb82026-05-11WarningsExact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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