FDA.reportPublic FDA data

Meloxicam

Product NDC
64205-127
11-digit product format
642050127
Labeler code
64205
Product ID
64205-127_c52473b6-90bb-4cdf-bd43-595b27ec6ab0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meloxicam
Dosage form
TABLET
Route
ORAL
Labeler
ReadyMeds
Application
ANDA077918
Marketing category
ANDA
Marketing start
2010-06-30
Marketing end
0000-00-00
Substance
MELOXICAM
Active strength
15 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

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
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64205-127-302019-11-27C16284748780-19855e2a2-4bed-60a7-e053-dbdaa90a05bdThese highlights do not include all the information needed to use Meloxicam Tablets, USP safely and effectively. See full prescribing information for Meloxicam Tablets, USP. Meloxicam Tablets, USP Initial U.S. Approval: 2000

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64205-127-30Meloxicam30 in 1 BOTTLE, PLASTICTABLET3010

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MeloxicamACTIVE INGREDIENTVG2QF83CGLMELOXICAM TABLET [READYMEDS]10
MeloxicamACTIVE MOIETYVG2QF83CGLMELOXICAM TABLET [READYMEDS]10
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UMELOXICAM TABLET [READYMEDS]10
Colloidal Silicon DioxideINACTIVE INGREDIENTETJ7Z6XBU4MELOXICAM TABLET [READYMEDS]10
LactoseINACTIVE INGREDIENTJ2B2A4N98GMELOXICAM TABLET [READYMEDS]10
Magnesium StearateINACTIVE INGREDIENT70097M6I30MELOXICAM TABLET [READYMEDS]10
Povidone K30INACTIVE INGREDIENTU725QWY32XMELOXICAM TABLET [READYMEDS]10
Sodium CitrateINACTIVE INGREDIENT1Q73Q2JULRMELOXICAM TABLET [READYMEDS]10
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2MELOXICAM TABLET [READYMEDS]10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64205-127MELOXICAM TABLET [READYMEDS]10Legacy NDC, 1 package rows20140701_8b2aa351-4ac3-4b5f-a20c-060805812cd0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
152695meloxicam 15 MG Oral TabletPSN8b2aa351-4ac3-4b5f-a20c-060805812cd010
311486meloxicam 7.5 MG Oral TabletPSN8b2aa351-4ac3-4b5f-a20c-060805812cd010
152695meloxicam 15 MG Oral TabletSCD8b2aa351-4ac3-4b5f-a20c-060805812cd010
311486meloxicam 7.5 MG Oral TabletSCD8b2aa351-4ac3-4b5f-a20c-060805812cd010

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
64205-127-306420501273030 in 1 BOTTLE, PLASTICHistorical