MELOXICAM

Product NDC
71335-2327
11-digit product format
713352327
Labeler code
71335
Product ID
71335-2327_9e73d381-68bd-4c4a-926d-78ce6b4a5ee0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077929
Marketing category
ANDA
Marketing start
2006-07-19
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
71335-2327-07133523270020 TABLET in 1 BOTTLE (71335-2327-0) 20 tablet2024-01-08NoNoHistorical
71335-2327-17133523270130 TABLET in 1 BOTTLE (71335-2327-1) 30 tablet2024-01-08NoNoHistorical
71335-2327-27133523270260 TABLET in 1 BOTTLE (71335-2327-2) 60 tablet2024-01-08NoNoHistorical
71335-2327-37133523270390 TABLET in 1 BOTTLE (71335-2327-3) 90 tablet2024-01-08NoNoHistorical
71335-2327-47133523270414 TABLET in 1 BOTTLE (71335-2327-4) 14 tablet2024-01-08NoNoHistorical
71335-2327-571335232705100 TABLET in 1 BOTTLE (71335-2327-5) 100 tablet2024-01-08NoNoHistorical
71335-2327-6713352327067 TABLET in 1 BOTTLE (71335-2327-6) 7 tablet2024-01-08NoNoHistorical
71335-2327-77133523270710 TABLET in 1 BOTTLE (71335-2327-7) 10 tablet2024-01-08NoNoHistorical
71335-2327-87133523270815 TABLET in 1 BOTTLE (71335-2327-8) 15 tablet2024-01-08NoNoHistorical
71335-2327-97133523270928 TABLET in 1 BOTTLE (71335-2327-9) 28 tablet2024-01-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
MELOXICAMBryant Ranch Prepack2024-08-08HUMAN PRESCRIPTION DRUG LABEL102