Meloxicam

Product NDC
71610-542
11-digit product format
716100542
Labeler code
71610
Product ID
71610-542_c7a932c0-6588-459a-bbcc-222f304fe61b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA077918
Marketing category
ANDA
Marketing start
2010-06-30
Substance
MELOXICAM
Active strength
15 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
VG2QF83CGLMELOXICAM71125-38-7MELOXICAM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71610-542-307161005423030 TABLET in 1 BOTTLE, PLASTIC (71610-542-30) 30 tablet2021-04-13NoNoHistorical
71610-542-607161005426090 TABLET in 1 BOTTLE, PLASTIC (71610-542-60) 90 tablet2021-05-13NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
MeloxicamAphena Pharma Solutions - Tennessee, LLC2021-05-20HUMAN PRESCRIPTION DRUG LABEL1