MELOXICAM

Product NDC
58118-1158
11-digit product format
581181158
Labeler code
58118
Product ID
58118-1158_b0108fbf-a392-1917-e053-2a95a90abb1e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
Clinical Solutions Wholesale, LLC
Application
ANDA077929
Marketing category
ANDA
Marketing start
2006-07-19
Marketing end
0000-00-00
Substance
MELOXICAM
Active strength
8 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58118-1158-82024-01-30C16284748780-11030e365-564b-111a-e063-dadaa90a10e20df81730-d682-4afc-95ba-d804f9461732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58118-1158MELOXICAM TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC]4Legacy NDC20200925_0df81730-d682-4afc-95ba-d804f9461732.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58118-1158-85811811580830 TABLET in 1 BLISTER PACK (58118-1158-8) 30 tablet2018-02-070000-00-00NoNoCurrent