Meclizine Hydrochloride (Page 2 of 2)

PRINCIPAL DISPLAY PANEL – 25 mg, 30 Tablets

Meclizine Hydrochloride Tablets USP, 25 mg

25 mg

Rx Only

30 Tablets

label
(click image for full-size original)
MECLIZINE HYDROCHLORIDE
meclizine hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:12634-424(NDC:42806-014)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MECLIZINE HYDROCHLORIDE (MECLIZINE) MECLIZINE HYDROCHLORIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
LACTOSE MONOHYDRATE
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
Product Characteristics
Color white Score no score
Shape OVAL Size 13mm
Flavor Imprint Code E14
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:12634-424-00 10 TABLET in 1 BOTTLE None
2 NDC:12634-424-01 100 TABLET in 1 BOTTLE None
3 NDC:12634-424-09 35 TABLET in 1 BOTTLE None
4 NDC:12634-424-12 120 TABLET in 1 BOTTLE None
5 NDC:12634-424-18 180 TABLET in 1 BOTTLE None
6 NDC:12634-424-40 40 TABLET in 1 BOTTLE None
7 NDC:12634-424-42 42 TABLET in 1 BOTTLE None
8 NDC:12634-424-45 45 TABLET in 1 BOTTLE None
9 NDC:12634-424-50 50 TABLET in 1 BOTTLE None
10 NDC:12634-424-52 12 TABLET in 1 BLISTER PACK None
11 NDC:12634-424-54 14 TABLET in 1 BLISTER PACK None
12 NDC:12634-424-57 20 TABLET in 1 BLISTER PACK None
13 NDC:12634-424-59 30 TABLET in 1 BLISTER PACK None
14 NDC:12634-424-60 60 TABLET in 1 BOTTLE None
15 NDC:12634-424-61 10 TABLET in 1 BLISTER PACK None
16 NDC:12634-424-63 3 TABLET in 1 BLISTER PACK None
17 NDC:12634-424-66 6 TABLET in 1 BLISTER PACK None
18 NDC:12634-424-67 7 TABLET in 1 BLISTER PACK None
19 NDC:12634-424-69 9 TABLET in 1 BLISTER PACK None
20 NDC:12634-424-71 30 TABLET in 1 BOTTLE None
21 NDC:12634-424-74 24 TABLET in 1 BOTTLE None
22 NDC:12634-424-78 28 TABLET in 1 BOTTLE None
23 NDC:12634-424-79 25 TABLET in 1 BOTTLE None
24 NDC:12634-424-80 20 TABLET in 1 BOTTLE None
25 NDC:12634-424-81 21 TABLET in 1 BOTTLE None
26 NDC:12634-424-82 12 TABLET in 1 BOTTLE None
27 NDC:12634-424-84 14 TABLET in 1 BOTTLE None
28 NDC:12634-424-85 15 TABLET in 1 BOTTLE None
29 NDC:12634-424-90 90 TABLET in 1 BOTTLE None
30 NDC:12634-424-91 1 TABLET in 1 BLISTER PACK None
31 NDC:12634-424-92 2 TABLET in 1 BOTTLE None
32 NDC:12634-424-93 3 TABLET in 1 BOTTLE None
33 NDC:12634-424-94 4 TABLET in 1 BOTTLE None
34 NDC:12634-424-95 5 TABLET in 1 BOTTLE None
35 NDC:12634-424-96 6 TABLET in 1 BOTTLE None
36 NDC:12634-424-97 7 TABLET in 1 BOTTLE None
37 NDC:12634-424-98 8 TABLET in 1 BOTTLE None
38 NDC:12634-424-99 9 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA200294 04/30/2012
Labeler — Apotheca Inc. (051457844)
Establishment
Name Address ID/FEI Operations
Apotheca Inc. 051457844 relabel (12634-424), repack (12634-424)

Revised: 01/2017 Apotheca Inc.

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