Citalopram Hydrobromide (Page 8 of 8)

PRINCIPAL DISPLAY PANEL

Citalopram Tablets USP 40 mg:

label
(click image for full-size original)
CITALOPRAM HYDROBROMIDE citalopram hydrobromide tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:12634-027(NDC:13668-011)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CITALOPRAM HYDROBROMIDE (CITALOPRAM) CITALOPRAM 40 mg
Product Characteristics
Color brown (Tin) Score 2 pieces
Shape OVAL (oval,biconvex) Size 11mm
Flavor Imprint Code 4;0;1011
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:12634-027-00 10 TABLET in 1 BOTTLE None
2 NDC:12634-027-01 100 TABLET in 1 BOTTLE None
3 NDC:12634-027-09 35 TABLET in 1 BOTTLE None
4 NDC:12634-027-40 40 TABLET in 1 BOTTLE None
5 NDC:12634-027-42 42 TABLET in 1 BOTTLE None
6 NDC:12634-027-50 50 TABLET in 1 BOTTLE None
7 NDC:12634-027-52 12 TABLET in 1 BLISTER PACK None
8 NDC:12634-027-54 14 TABLET in 1 BLISTER PACK None
9 NDC:12634-027-57 20 TABLET in 1 BLISTER PACK None
10 NDC:12634-027-59 30 TABLET in 1 BLISTER PACK None
11 NDC:12634-027-60 60 TABLET in 1 BOTTLE None
12 NDC:12634-027-61 10 TABLET in 1 BLISTER PACK None
13 NDC:12634-027-63 3 TABLET in 1 BLISTER PACK None
14 NDC:12634-027-66 6 TABLET in 1 BLISTER PACK None
15 NDC:12634-027-67 7 TABLET in 1 BLISTER PACK None
16 NDC:12634-027-69 9 TABLET in 1 BLISTER PACK None
17 NDC:12634-027-71 30 TABLET in 1 BOTTLE None
18 NDC:12634-027-74 24 TABLET in 1 BOTTLE None
19 NDC:12634-027-78 28 TABLET in 1 BOTTLE None
20 NDC:12634-027-79 25 TABLET in 1 BOTTLE None
21 NDC:12634-027-80 20 TABLET in 1 BOTTLE None
22 NDC:12634-027-81 21 TABLET in 1 BOTTLE None
23 NDC:12634-027-82 12 TABLET in 1 BOTTLE None
24 NDC:12634-027-85 15 TABLET in 1 BOTTLE None
25 NDC:12634-027-91 1 TABLET in 1 BLISTER PACK None
26 NDC:12634-027-94 4 TABLET in 1 BOTTLE None
27 NDC:12634-027-95 5 TABLET in 1 BOTTLE None
28 NDC:12634-027-96 6 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078216 10/18/2007
Labeler — Apotheca Inc. (051457844)
Establishment
Name Address ID/FEI Operations
Apotheca Inc. 051457844 relabel (12634-027), repack (12634-027)

Revised: 06/2016 Apotheca Inc.

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