Meloxicam

Product NDC
70934-297
11-digit product format
709340297
Labeler code
70934
Product ID
70934-297_a5654132-ca5e-f592-e053-2a95a90a69eb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Application
ANDA077918
Marketing category
ANDA
Marketing start
2019-02-26
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#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70934-297-307093402973030 TABLET in 1 BOTTLE, PLASTIC (70934-297-30) 30 tablet2019-02-260000-00-00NoNoCurrent
70934-297-607093402976060 TABLET in 1 BOTTLE, PLASTIC (70934-297-60) 60 tablet2019-03-250000-00-00NoNoCurrent
70934-297-907093402979090 TABLET in 1 BOTTLE, PLASTIC (70934-297-90) 90 tablet2020-04-280000-00-00NoNoCurrent