FDA.reportPublic FDA data

NDC 60793-602-02 - BICILLIN C-R 900/300

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
60793-602
Requested NDC
60793-602-02
Package NDCs from labels
60793-602-02, 60793-602-10
Manufacturer
Pfizer Laboratories Div Pfizer Inc | King Pharmaceuticals LLC
Effective date
2026-07-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PENICILLIN G - Pfizer Laboratories Div Pfizer Inc | King Pharmaceuticals LLCPfizer Laboratories Div Pfizer Inc | King Pharmaceuticals LLC2026-07-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60793-602-02BICILLIN C-R 900/3002 mL in 1 SYRINGEINJECTION, SUSPENSION231
60793-602-10BICILLIN C-R 900/30010 in 1 PACKAGEINJECTION, SUSPENSION1031

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60793-602BICILLIN C-R 900/300 (PENICILLIN G BENZATHINE AND PENICILLIN G PROCAINE) INJECTION, SUSPENSION [PFIZER LABORATORIES DIV PFIZER INC]31Current NDC, Legacy NDC, 2 package rows20240606_ba7b9199-4710-4189-a85d-77ed75befe4d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60793-602-02ML - Milliliter60793-602b817c2e5-42cd-4af7-bddd-9f8bbf1e314712014-11-05
60793-602-10ML - Milliliter60793-6025bf2c7fa-3de4-483e-9817-817cfb3f671912012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PENICILLIN G BENZATHINEACTIVE INGREDIENTRIT82F58GKBICILLIN C-R 900/300 (PENICILLIN G BENZATHINE AND PENICILLIN G PROCAINE) INJECTION, SUSPENSION [PFIZER LABORATORIES DIV PFIZER INC]13
PENICILLIN G PROCAINEACTIVE INGREDIENT17R794ESYNBICILLIN C-R 900/300 (PENICILLIN G BENZATHINE AND PENICILLIN G PROCAINE) INJECTION, SUSPENSION [PFIZER LABORATORIES DIV PFIZER INC]13
PENICILLIN GACTIVE MOIETYQ42T66VG0CBICILLIN C-R 900/300 (PENICILLIN G BENZATHINE AND PENICILLIN G PROCAINE) INJECTION, SUSPENSION [PFIZER LABORATORIES DIV PFIZER INC]13

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 5 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BICILLIN C-R 900/300PENICILLIN G BENZATHINE AND PENICILLIN G PROCAINEPfizer Laboratories Div Pfizer Incba7b9199-4710-4189-a85d-77ed75befe4d2026-07-21Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA050138
ndc (package): 60793-602-10
ndc (package): 60793-602-02
ndc (product): 60793-602
ndc11 (package): 60793060202
rxcui: 836306
rxcui: 836307
spl id: 18e5ae26-c3f5-4d22-8657-fd767cadc25f
spl set id: ba7b9199-4710-4189-a85d-77ed75befe4d
unii: 17R794ESYN
unii: RIT82F58GK
BICILLIN L-APENICILLIN G BENZATHINEPfizer Laboratories Div Pfizer Inc012d46f1-d0a0-4676-a879-cd320297ab162026-07-21Boxed warning, Warnings, Adverse reactionsExact identifier
unii: RIT82F58GK
BICILLIN CRPENICILLIN G BENZATHINE AND PENICILLIN G PROCAINEPfizer Laboratories Div Pfizer Incb5640fc6-76d8-428d-80e6-760d769af8bb2026-07-21Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA050138
unii: 17R794ESYN
unii: RIT82F58GK
LentocilinPENICILLIN G BENZATHINLABORATRIOS ATRAL, S.A.1a4e5124-618b-ce44-e063-6394a90a43e32024-06-07Warnings, Adverse reactionsExact identifier
unii: RIT82F58GK
BICILLIN L-APENICILLIN G BENZATHINEA-S Medication Solutionsa519a9bf-8fec-4fd3-b0b2-f4ae8c7f20ce2023-10-24Boxed warning, Warnings, Adverse reactionsExact identifier
unii: RIT82F58GK

Reported adverse events (FAERS/openFDA)#

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