NDC 50742-310-50 - Mafenide Acetate

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
50742-310
Requested NDC
50742-310-50
Package NDCs from labels
50742-310-50, 50742-310-25
Manufacturer
Ingenus Pharmaceuticals, LLC | Novast Laboratories Ltd. | Sharp Corporation
Effective date
2023-12-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Mafenide Acetate for Topical Solution USP, 5% STERILE Rx OnlyIngenus Pharmaceuticals, LLC | Novast Laboratories Ltd. | Sharp Corporation2023-12-05HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50742-310-25EA - Each50742-3106145b7e5-b01b-4eb0-862b-9ded9bee966212018-11-06
50742-310-50EA - Each50742-310e81bc6af-019e-4317-ad9e-6a0ee8d33ab212019-03-12

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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
35c3308c-dd1f-4eed-955b-5f8ad4732a0b3f397e17-d14d-4a8d-a44c-6f81cd9a7abd2023-12-05Warnings, Adverse reactionsExact identifier
spl id: 35c3308c-dd1f-4eed-955b-5f8ad4732a0b
spl set id: 3f397e17-d14d-4a8d-a44c-6f81cd9a7abd
SULFAMYLONMAFENIDE ACETATERising Pharma Holdings, Inc.008eaa23-8f19-4e39-85ff-540c1c834a9e2023-07-03Warnings, Adverse reactionsExact identifier
unii: RQ6LP6Z0WY

Reported adverse events (FAERS/openFDA)#

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