FDA.reportPublic FDA data

NDC 49502-101-01 - Epinephrine

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
49502-101
Requested NDC
49502-101-01
Package NDCs from labels
49502-101-01, 49502-101-02
Manufacturer
Sportpharm LLC
Effective date
2026-10-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Epinephrine - Sportpharm LLCSportpharm LLC2026-10-12HUMAN PRESCRIPTION DRUG LABEL
Epinephrine 0.15 Pediatrics - Sina Health IncSina Health Inc2026-01-12HUMAN PRESCRIPTION DRUG LABEL
Epinephrine - REMEDYREPACK INC.REMEDYREPACK INC.2024-02-23HUMAN PRESCRIPTION DRUG LABEL
Epinephrine - Medical Purchasing Solutions, LLCMedical Purchasing Solutions, LLC2023-05-22HUMAN PRESCRIPTION DRUG LABEL
Epinephrine - Viatris Specialty LLCViatris Specialty LLC2023-02-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49502-101-01Epinephrine0.3 mL in 1 SYRINGE, GLASSINJECTION0.335
49502-101-01Epinephrine1 in 1 CONTAINERINJECTION135
49502-101-02Epinephrine2 in 1 CARTONINJECTION235

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49502-101EPINEPHRINE INJECTION [VIATRIS SPECIALTY LLC]35Current NDC, Legacy NDC, 3 package rows20250215_778ac6ae-6bcb-47a4-bcb3-8dd0da9f8836.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49502-101-01EA - Each49502-1013a1cad26-62d8-4cf0-a0cc-a5b82b77252112017-06-15
49502-101-02EA - Each49502-101740e8b3a-e2ef-4dd9-ac99-29864b0cd1e312017-03-06

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 63 of 63 · 1,242 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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.