Meloxicam

Product NDC: 66116-443
11-digit product format: 661160443
Labeler code: 66116
Product ID: 66116-443_d224143d-2199-4969-a64f-dc2e6b865ec4
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Meloxicam
Dosage form: TABLET
Route: ORAL
Labeler: MedVantx, Inc.
Application: ANDA077936
Marketing category: ANDA
Marketing start: 2006-07-20
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 concept	Relation	Version	Effective
bdef11ce-16e2-4690-96a3-597bcf5cc738	Product name	1	20260130
f2791553-0b76-42f4-8d49-af3eda072bfb	Product name	1	20251117
e3a99641-4540-4894-9108-00cab3c57b7e	Product name	1	20211207
3e9b4ed6-844c-4725-9d19-cceb5c823572	Product name	2	20210903
b21a682e-c765-4e26-9bb2-dbb8c7b38ef7	Product name	1	20200623
a428d1db-64d7-4fc3-8d13-832b1e84b683	Product name	1	20190201
96649a58-aac8-401c-be00-450b4335f7e7	Product name	1	20161116
f0761cb7-8207-3a19-2ca3-ecbb559b04e1	Product name	2	20161116

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
66116-443-30	2019-11-27	C162847	48780-1	9855d018-dc2e-cd31-e053-dbdaa90ab51a	These 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 for oral use Initial U.S. Approval: 2000

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
66116-443-30	Meloxicam	30 in 1 BOTTLE	TABLET	30		1

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
66116-443-30	EA - Each	66116-443	03d4f78c-0ee8-4ab7-b69f-b4a9b535a285	1	2014-09-03

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MELOXICAM	ACTIVE INGREDIENT	VG2QF83CGL	MELOXICAM TABLET [MEDVANTX, INC.]	1
MELOXICAM	ACTIVE MOIETY	VG2QF83CGL	MELOXICAM TABLET [MEDVANTX, INC.]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	MELOXICAM TABLET [MEDVANTX, INC.]	1
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	MELOXICAM TABLET [MEDVANTX, INC.]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	MELOXICAM TABLET [MEDVANTX, INC.]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MELOXICAM TABLET [MEDVANTX, INC.]	1
POVIDONE K30	INACTIVE INGREDIENT	U725QWY32X	MELOXICAM TABLET [MEDVANTX, INC.]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	MELOXICAM TABLET [MEDVANTX, INC.]	1
TRISODIUM CITRATE DIHYDRATE	INACTIVE INGREDIENT	B22547B95K	MELOXICAM TABLET [MEDVANTX, INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66116-443	MELOXICAM TABLET [MEDVANTX, INC.]	1	Legacy NDC, 1 package rows	20130821_d224143d-2199-4969-a64f-dc2e6b865ec4.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
VG2QF83CGL	MELOXICAM	71125-38-7	MELOXICAM

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
152695	meloxicam 15 MG Oral Tablet	PSN	d224143d-2199-4969-a64f-dc2e6b865ec4	1
152695	meloxicam 15 MG Oral Tablet	SCD	d224143d-2199-4969-a64f-dc2e6b865ec4	1

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Status
66116-443-30	66116044330	30 in 1 BOTTLE	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Meloxicam	MedVantx, Inc. \| Teva Pharmaceuticals USA Inc \| Blenheim Pharmacal, Inc.	2013-04-25	HUMAN PRESCRIPTION DRUG LABEL	1