FDA.reportPublic FDA data

NDC 70518-1808-00 - mupirocin

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
70518-1808
Requested NDC
70518-1808-00
Package NDCs from labels
70518-1808-0, 70518-1808-00
Manufacturer
REMEDYREPACK INC.
Effective date
2026-01-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
mupirocin - REMEDYREPACK INC.REMEDYREPACK INC.2026-01-28HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-1808-0mupirocin1 in 1 CARTONOINTMENT18
70518-1808-0mupirocin22 g in 1 TUBEOINTMENT228

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-1808MUPIROCIN OINTMENT [REMEDYREPACK INC.]6Current NDC, Legacy NDC, 2 package rows20250228_290b4e51-59b4-429a-987b-715ac817ef2c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-1808-0GM - Gram70518-18086af69c87-4cd3-4871-a6a0-439e41a4aa3112026-01-08

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 2 of 2 · 33 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MupirocinMUPIROCINAdvanced Rx Pharmacy of Tennessee, LLCf1a048d9-af57-a4a2-e053-2995a90a86632024-12-31Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
MupirocinMUPIROCINAdvanced Rx Pharmacy of Tennessee, LLCf1a01044-8f2e-4e91-e053-2995a90af7222024-12-31Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
DermacinRx ClorhexacinMUPIROCIN OINTMENTPureTek Corporation3c8cb9a6-58e5-4e8d-bfdc-1432a1bde6f92024-12-13Warnings, Adverse reactionsExact identifier
rxcui: 106346
MupirocinMUPIROCINNuCare Pharmaceuticals,Inc.66db1071-024f-aa19-e053-2a91aa0a8e392024-06-06Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
mupirocinMUPIROCINA-S Medication Solutionsa6c22c25-0f02-4c06-bbc2-723a18ecdda82024-01-30Warnings, Adverse reactionsExact identifier
application number: ANDA065123
rxcui: 106346
unii: D0GX863OA5
mupirocinMUPIROCINPadagis Israel Pharmaceuticals Ltde9b61f01-3c67-42a4-a62b-10f1d13431902023-12-31Warnings, Adverse reactionsExact identifier
application number: ANDA065123
ndc (product): 45802-112
rxcui: 106346
spl id: d51e7348-2495-41d4-93c1-bfaef2dac375
spl set id: e9b61f01-3c67-42a4-a62b-10f1d1343190
unii: D0GX863OA5
MupirocinMUPIROCINProficient Rx LP2777e4f2-2b8d-41f5-a96a-02dec8c7c3e02023-11-01Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
mupirocinMUPIROCINBryant Ranch Prepack1cd4c71f-138b-47c2-8ce8-9ac32408dc562023-07-18Warnings, Adverse reactionsExact identifier
application number: ANDA065123
rxcui: 106346
unii: D0GX863OA5
MupirocinMUPIROCINProficient Rx LPd8766748-6b53-4673-a3ee-5cd8a43016472023-01-01Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
MupirocinMUPIROCINProficient Rx LPcbb18010-f3b5-4ed7-8c03-c9203f0e360e2022-10-01Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
MupirocinMUPIROCINTeva Pharmaceuticals USA, Inc.a543797a-2c1c-4ea3-bd6c-227a784f92d92022-05-01Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
mupirocinMUPIROCINProficient Rx LP97f8d67d-c422-4a26-9394-24a5ec9719d92022-04-01Warnings, Adverse reactionsExact identifier
application number: ANDA065123
rxcui: 106346
unii: D0GX863OA5
mupirocinMUPIROCINAsclemed USA, Inc.b2ff9c56-ca19-48ca-bd08-4b33edb13a082020-11-09Warnings, Adverse reactionsExact identifier
application number: ANDA065123
rxcui: 106346
unii: D0GX863OA5

Reported adverse events (FAERS/openFDA)#

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