FDA.reportPublic FDA data

Meloxicam

Product NDC
50268-526
11-digit product format
502680526
Labeler code
50268
Product ID
50268-526_3eecb0bf-b1c0-14ba-e063-6394a90a14ce
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
AvPAK
Application
ANDA077918
Marketing category
ANDA
Marketing start
2012-10-09
Substance
MELOXICAM
Active strength
15 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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Meloxicam
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MELOXICAM15 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiVG2QF83CGL
Rxcui152695, 311486

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bdef11ce-16e2-4690-96a3-597bcf5cc738Product name120260130
f2791553-0b76-42f4-8d49-af3eda072bfbProduct name120251117
e3a99641-4540-4894-9108-00cab3c57b7eProduct name120211207
3e9b4ed6-844c-4725-9d19-cceb5c823572Product name220210903
b21a682e-c765-4e26-9bb2-dbb8c7b38ef7Product name120200623
a428d1db-64d7-4fc3-8d13-832b1e84b683Product name120190201
96649a58-aac8-401c-be00-450b4335f7e7Product name120161116
f0761cb7-8207-3a19-2ca3-ecbb559b04e1Product name220161116

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50268-526-11Meloxicam1 in 1 BLISTER PACKTABLET110
50268-526-15Meloxicam50 in 1 BOX, UNIT-DOSETABLET5010

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50268-526-11EA - Each50268-5267bafddba-257d-47eb-bc61-a25a11c90c3912015-04-03
50268-526-15EA - Each50268-52644decdea-dc2e-4ecb-b93f-6ef1e9c21b8712013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MeloxicamACTIVE INGREDIENTVG2QF83CGLMELOXICAM (MELOXICAM) TABLET [AVPAK]4
MeloxicamACTIVE MOIETYVG2QF83CGLMELOXICAM (MELOXICAM) TABLET [AVPAK]4
Cellulose, MicrocrystallineINACTIVE INGREDIENTOP1R32D61UMELOXICAM (MELOXICAM) TABLET [AVPAK]4
LactoseINACTIVE INGREDIENTJ2B2A4N98GMELOXICAM (MELOXICAM) TABLET [AVPAK]4
Magnesium StearateINACTIVE INGREDIENT70097M6I30MELOXICAM (MELOXICAM) TABLET [AVPAK]4
Povidone K30INACTIVE INGREDIENTU725QWY32XMELOXICAM (MELOXICAM) TABLET [AVPAK]4
Silicon DioxideINACTIVE INGREDIENTETJ7Z6XBU4MELOXICAM (MELOXICAM) TABLET [AVPAK]4
Sodium CitrateINACTIVE INGREDIENT1Q73Q2JULRMELOXICAM (MELOXICAM) TABLET [AVPAK]4
Sodium Starch Glycolate Type A PotatoINACTIVE INGREDIENT5856J3G2A2MELOXICAM (MELOXICAM) TABLET [AVPAK]4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50268-526MELOXICAM TABLET [AVPAK]9Current NDC, Legacy NDC, 2 package rows20240110_ee8df8fa-d08a-8c8b-f048-813e5022a101.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
152695meloxicam 15 MG Oral TabletPSNee8df8fa-d08a-8c8b-f048-813e5022a10110
311486meloxicam 7.5 MG Oral TabletPSNee8df8fa-d08a-8c8b-f048-813e5022a10110
152695meloxicam 15 MG Oral TabletSCDee8df8fa-d08a-8c8b-f048-813e5022a10110
311486meloxicam 7.5 MG Oral TabletSCDee8df8fa-d08a-8c8b-f048-813e5022a10110

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50268-526-11502680526111 in 1 BLISTER PACKHistorical
50268-526-155026805261550 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-526-15) / 1 TABLET in 1 BLISTER PACK (50268-526-11) 50 blister pack2012-10-090000-00-00NoNoCurrent