NDC 70771-1350-2 - methylprednisolone

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
70771-1350
Requested NDC
70771-1350-2
Package NDCs from labels
70771-1350-7, 70771-1350-1, 70771-1350-5, 70771-1350-2, 70771-1350-4
Manufacturer
Zydus Lifesciences Limited
Effective date
2024-12-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
methylprednisolone - Zydus Lifesciences LimitedZydus Lifesciences Limited2024-12-05HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70771-1350-1methylprednisolone100 in 1 BOTTLETABLET1008
70771-1350-2methylprednisolone10 in 1 BLISTER PACKTABLET108
70771-1350-4methylprednisolone10 in 1 CARTONTABLET108
70771-1350-5methylprednisolone500 in 1 BOTTLETABLET5008
70771-1350-7methylprednisolone50 in 1 BOTTLETABLET508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70771-1350METHYLPREDNISOLONE TABLET [ZYDUS LIFESCIENCES LIMITED]8Current NDC, Legacy NDC, 5 package rows20241207_fe9c15b5-4264-45f1-87b5-f7e1d6e6ddee.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 3 of 3 · 42 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
METHYLPREDNISOLONEMETHYLPREDNISOLONEDoc Rxc6ec50b5-aeb8-40c3-83e2-af4fe8fefb142021-06-11Warnings, Adverse reactionsExact identifier
rxcui: 259966
unii: X4W7ZR7023
METHYLPREDNISOLONEMETHYLPREDNISOLONEAsclemed USA, Inc.8bff5330-c1f6-4014-aadb-45c1726248dd2021-03-16Warnings, Adverse reactionsExact identifier
rxcui: 259966
unii: X4W7ZR7023

Reported adverse events (FAERS/openFDA)#

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