Meloxicam

Product NDC
63629-6707
11-digit product format
636296707
Labeler code
63629
Product ID
63629-6707_5edffe5b-cc2f-4a96-9a7f-ac5b8e8418bf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077944
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#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-6707-16362967070160 TABLET in 1 BOTTLE (63629-6707-1) 60 tablet2015-08-280000-00-00NoNoCurrent
63629-6707-26362967070230 TABLET in 1 BOTTLE (63629-6707-2) 30 tablet2015-08-280000-00-00NoNoCurrent