NDC Code(s) : 49349-709-20
Packager : REMEDYREPACK INC.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

MeloxicamMeloxicam TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:49349-709
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELOXICAM(UNII: VG2QF83CGL)
(MELOXICAM - UNII:VG2QF83CGL) 		MELOXICAM15 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE(UNII: OP1R32D61U)
MAGNESIUM STEARATE(UNII: 70097M6I30)
POVIDONE K30(UNII: U725QWY32X)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
LACTOSE(UNII: J2B2A4N98G)
SODIUM CITRATE(UNII: 1Q73Q2JULR)
SODIUM STARCH GLYCOLATE TYPE A POTATO(UNII: 5856J3G2A2)
Product Characteristics
Color yellow Score no score
Shape ROUND (TABLET) Size 8 mm
Flavor Imprint Code 100
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:49349-709-20100 in 1 VIAL Type 0: Not a Combination Product03/01/2013
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077918 01/03/2013 08/25/2016

PRINCIPAL DISPLAY PANEL

DRUG: Meloxicam


GENERIC: Meloxicam


DOSAGE: TABLET


ADMINSTRATION: ORAL


NDC: 49349-709-20


ACTIVE INGREDIENT(S):

  • Meloxicam 15mg in 1


INACTIVE INGREDIENT(S):

  • Cellulose, Microcrystalline
  • Magnesium Stearate
  • Povidone K30
  • Silicon Dioxide
  • Lactose
  • Sodium Citrate
  • Sodium Starch Glycolate Type A Potato


COLOR: yellow


SHAPE: ROUND


SCORE: No score


SIZE: 8 mm


IMPRINT: 100


PACKAGING: 100 in 1 VIAL



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