NDC Code(s) : 52389-623-24
Packager : Alva-Amco Pharmacal Companies, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Verticalm Meclizine Hydrochloride TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52389-623
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MECLIZINE HYDROCHLORIDE(UNII: HDP7W44CIO)
(MECLIZINE - UNII:3L5TQ84570) 		MECLIZINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN(UNII: O8232NY3SJ)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
D&C YELLOW NO. 10(UNII: 35SW5USQ3G)
Lactose(UNII: J2B2A4N98G)
Magnesium stearate(UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE(UNII: OP1R32D61U)
Silicon dioxide(UNII: ETJ7Z6XBU4)
Stearic acid(UNII: 4ELV7Z65AP)
Product Characteristics
Color yellow (yellow) Score no score
Shape ROUND Size 9 mm
Flavor Imprint Code ALVA
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:52389-623-241 in 1 CARTON
124 in 1 BLISTER PACK
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part336 04/16/2012

PRINCIPAL DISPLAY PANEL

Verticalm PDP