MELOXICAM

Product NDC
68071-1919
11-digit product format
680711919
Labeler code
68071
Product ID
68071-1919_d8510e16-33c8-778a-e053-2995a90a31a5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA077929
Marketing category
ANDA
Marketing start
2006-07-19
Marketing end
0000-00-00
Substance
MELOXICAM
Active strength
8 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
2023-12-31
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
68071-1919-26807119190220 TABLET in 1 BOTTLE (68071-1919-2) 20 tablet2017-02-210000-00-00NoNoCurrent
68071-1919-36807119190330 TABLET in 1 BOTTLE (68071-1919-3) 30 tablet2017-02-210000-00-00NoNoCurrent
68071-1919-56807119190515 TABLET in 1 BOTTLE (68071-1919-5) 15 tablet2017-02-210000-00-00NoNoCurrent
68071-1919-66807119190660 TABLET in 1 BOTTLE (68071-1919-6) 60 tablet2017-02-210000-00-00NoNoCurrent
68071-1919-96807119190990 TABLET in 1 BOTTLE (68071-1919-9) 90 tablet2017-02-210000-00-00NoNoCurrent