NDC 83270-002-01 - Carboprost Tromethamine

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
83270-002
Requested NDC
83270-002-01
Package NDCs from labels
83270-002-10, 83270-002-01, 83270-002-02
Manufacturer
ONESOURCE SPECIALTY PHARMA LIMITED | Onesource Specialty Pte. Limited
Effective date
2025-08-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Carboprost Tromethamine - ONESOURCE SPECIALTY PHARMA LIMITED | Onesource Specialty Pte. LimitedONESOURCE SPECIALTY PHARMA LIMITED | Onesource Specialty Pte. Limited2025-08-29HUMAN PRESCRIPTION DRUG LABEL
Carboprost Tromethamine - ONESOURCE SPECIALTY PHARMA LIMITED | Onesource Specialty Pte. LimitedONESOURCE SPECIALTY PHARMA LIMITED | Onesource Specialty Pte. Limited2025-05-22HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83270-002-10Carboprost Tromethamine10 in 1 CARTONINJECTION, SOLUTION101
83270-002-10Carboprost Tromethamine1 mL in 1 VIALINJECTION, SOLUTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83270-002CARBOPROST TROMETHAMINE INJECTION, SOLUTION [ONESOURCE SPECIALTY PHARMA LIMITED]3Current NDC20250523_6484c309-2041-4c25-a233-9d1fb6da583c.zip

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 44 of 44 · 864 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SODIUM CHLORIDESODIUM CHLORIDEBaxter Healthcare Corporationb3b4b176-41f0-4ca8-90d4-3fba5707564a2014-02-21Exact identifier
unii: 451W47IQ8X
TIS-U-SOLSODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATEBaxter Healthcare Corporation9da4121f-d62d-4da4-8dfb-0494da16015f2014-02-21Exact identifier
unii: 451W47IQ8X
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,Baxter Healthcare Corporatione1953d54-818d-46a6-8532-518ebae6d84e2012-06-13Exact identifier
unii: 451W47IQ8X
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDEBaxter Healthcare Corporationf09f80bf-2f8b-4420-865d-aec2d5e5cd4d2012-06-12Exact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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