FDA.reportPublic FDA data

NDC 0781-6153-94 - Penicillin G Sodium

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
0781-6153
Requested NDC
0781-6153-94
Package NDCs from labels
0781-6153-94, 0781-6153-95, 0781-6153-97
Manufacturer
Sandoz Inc
Effective date
2020-05-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Penicillin G Sodium - Sandoz IncSandoz Inc2020-05-27HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2012-07-24Indexing - Billing Unit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0781-6153-94Penicillin G Sodium1 in 1 VIALINJECTION, POWDER, FOR SOLUTION115
0781-6153-95Penicillin G Sodium10 in 1 CARTONINJECTION, POWDER, FOR SOLUTION1015
0781-6153-97Penicillin G Sodium1 in 1 VIALINJECTION, POWDER, FOR SOLUTION115
0781-6153-97Penicillin G Sodium50 in 1 CARTONINJECTION, POWDER, FOR SOLUTION5015

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0781-6153PENICILLIN G SODIUM INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]15Current NDC, Legacy NDC, 4 package rows20200605_23b6d4a3-b273-4e10-9da9-1376933fdbdf.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-6153-94EA - Each0781-615310b6ce8e-7539-4407-a3b1-f7c5176249c612012-07-24
0781-6153-95EA - Each0781-61535e5d1c94-31d1-4902-83e1-d182746eb5cf12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PENICILLIN G SODIUMACTIVE INGREDIENTYS5LY7JF4NPENICILLIN G SODIUM INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]12
PENICILLIN GACTIVE MOIETYQ42T66VG0CPENICILLIN G SODIUM INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]12

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 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Penicillin G SodiumPENICILLIN G SODIUMSandoz Inc23b6d4a3-b273-4e10-9da9-1376933fdbdf2020-05-27Warnings, Adverse reactionsExact identifier
application number: ANDA065068
ndc (package): 0781-6153-94
ndc (package): 0781-6153-95
ndc (package): 0781-6153-97
ndc (product): 0781-6153
ndc11 (package): 00781615394
rxcui: 745302
spl id: 0e84343e-8796-4c54-8dcc-8448a231fcfa
spl set id: 23b6d4a3-b273-4e10-9da9-1376933fdbdf
unii: YS5LY7JF4N

Reported adverse events (FAERS/openFDA)#

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