MELOXICAM

Product NDC
70518-1299
11-digit product format
705181299
Labeler code
70518
Product ID
70518-1299_e3b4f9b1-ac2b-cb2a-e053-2a95a90a9e1e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA077929
Marketing category
ANDA
Marketing start
2018-07-12
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-1299-0EA - Each70518-1299c4145345-6a64-46e8-bf97-71ae5bcd118912026-01-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-1299MELOXICAM TABLET [REMEDYREPACK INC.]16Legacy NDC20250510_c1bd7dae-d66f-41eb-84a3-3349f58d4700.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-1299-07051812990030 TABLET in 1 BOTTLE, PLASTIC (70518-1299-0) 30 tablet2018-07-120000-00-00NoNoCurrent
70518-1299-17051812990160 TABLET in 1 BOTTLE, PLASTIC (70518-1299-1) 60 tablet2018-08-080000-00-00NoNoCurrent
70518-1299-27051812990290 TABLET in 1 BOTTLE, PLASTIC (70518-1299-2) 90 tablet2019-10-030000-00-00NoNoCurrent