Meloxicam

Product NDC
72162-1738
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077918
Marketing category
ANDA
Substance
MELOXICAM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-1738-01000 TABLET in 1 BOTTLE, PLASTIC (72162-1738-0) 2024-02-06NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
MeloxicamBryant Ranch Prepack2025-04-01HUMAN PRESCRIPTION DRUG LABEL101