NDC 66794-251-02 - Erythromycin Lactobionate

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
66794-251
Requested NDC
66794-251-02
Package NDCs from labels
66794-251-02, 66794-251-41
Manufacturer
Piramal Critical Care Inc. | Gland Pharma Limited
Effective date
2026-08-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Erythromycin Lactobionate - Piramal Critical Care Inc. | Gland Pharma LimitedPiramal Critical Care Inc. | Gland Pharma Limited2026-08-16HUMAN PRESCRIPTION DRUG LABEL

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 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Erythromycin LactobionateERYTHROMYCIN LACTOBIONATEPiramal Critical Care Inc.ee345752-0f0c-c69b-e053-2995a90a7dac2026-08-16Warnings, Adverse reactionsExact identifier
application number: ANDA216761
ndc (package): 66794-251-41
ndc (package): 66794-251-02
ndc (product): 66794-251
ndc11 (package): 66794025102
rxcui: 1668264
spl id: 593675b3-e44e-0b1e-e063-6294a90a3ee7
spl set id: ee345752-0f0c-c69b-e053-2995a90a7dac
unii: 33H58I7GLQ
Erythromycin LactobionateERYTHROMYCIN LACTOBIONATEArmas Pharmaceuticals Inc.ca65a48f-5fe6-4b31-8359-51dbc31f6d4e2026-07-09Warnings, Adverse reactionsExact identifier
application number: ANDA216761
rxcui: 1668264
unii: 33H58I7GLQ
Erythrocin LactobionateERYTHROMYCIN LACTOBIONATEHospira, Inc.a96c405f-bd70-4bb4-719e-ac6a79dcc2132025-10-30Warnings, Adverse reactionsExact identifier
rxcui: 1668264
unii: 33H58I7GLQ
erythromycin lactobionateERYTHROMYCIN LACTOBIONATEGland Pharma Limitedc6f9565b-6d9d-40e3-87f8-9f38ede9173a2024-11-20Warnings, Adverse reactionsExact identifier
application number: ANDA216761
rxcui: 1668264
unii: 33H58I7GLQ

Reported adverse events (FAERS/openFDA)#

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