Meloxicam

Product NDC
70934-030
11-digit product format
709340030
Labeler code
70934
Product ID
70934-030_a70b07af-fd9e-d0a8-e053-2a95a90addf9
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
2017-03-27
Marketing end
0000-00-00
Substance
MELOXICAM
Active strength
15 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#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70934-030-30EA - Each70934-0307afbf2b1-e004-4fe1-bb56-4a093b25d73b12022-01-06
70934-030-90EA - Each70934-030a6d284c5-a67e-4f51-8e5a-84bd8c8b36f512022-12-07

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70934-030-147093400301414 TABLET in 1 BOTTLE, PLASTIC (70934-030-14) 14 tablet2017-03-270000-00-00NoNoCurrent
70934-030-307093400303030 TABLET in 1 BOTTLE, PLASTIC (70934-030-30) 30 tablet2019-03-070000-00-00NoNoCurrent
70934-030-607093400306060 TABLET in 1 BOTTLE, PLASTIC (70934-030-60) 60 tablet2020-05-280000-00-00NoNoCurrent
70934-030-907093400309090 TABLET in 1 BOTTLE, PLASTIC (70934-030-90) 90 tablet2020-04-240000-00-00NoNoCurrent