01 5ALENDRONATE SODIUM
02 2ALENDRONATE SODIUM; CHOLECALCIFEROL
03 4ATORVASTATIN CALCIUM; EZETIMIBE
04 1BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE
05 3BETAMETHASONE DIPROPIONATE
06 1BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
07 5CARBIDOPA; LEVODOPA
08 1CLINDAMYCIN PHOSPHATE
09 3DESLORATADINE
10 2DESLORATADINE; PSEUDOEPHEDRINE SULFATE
11 1ETHINYL ESTRADIOL; ETONOGESTREL
12 2ETONOGESTREL
13 1EZETIMIBE
14 4EZETIMIBE; SIMVASTATIN
15 2FINASTERIDE
16 3FORMOTEROL FUMARATE; MOMETASONE FUROATE
17 1GANIRELIX ACETATE
18 3HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
19 3LOSARTAN POTASSIUM
20 6MIRTAZAPINE
21 10MOMETASONE FUROATE
22 4MONTELUKAST SODIUM
23 4RIZATRIPTAN BENZOATE
24 5SIMVASTATIN
01 6AEROSOL, METERED;INHALATION
02 1CREAM, AUGMENTED;TOPICAL
03 3CREAM;TOPICAL
04 1GEL;VAGINAL
05 1GRANULE;ORAL
06 2IMPLANT;IMPLANTATION
07 2INJECTABLE;INJECTION
08 1LOTION, AUGMENTED;TOPICAL
09 1LOTION;TOPICAL
10 1OINTMENT, AUGMENTED;TOPICAL
11 1OINTMENT;TOPICAL
12 2POWDER;INHALATION
13 1RING;VAGINAL
14 1SPRAY, METERED;NASAL
15 2TABLET, CHEWABLE;ORAL
16 4TABLET, EXTENDED RELEASE;ORAL
17 7TABLET, ORALLY DISINTEGRATING;ORAL
18 39TABLET;ORAL
01 10.005MG/INH;0.05MG/INH
02 10.005MG/INH;0.1MG/INH
03 10.005MG/INH;0.2MG/INH
04 10.015MG/24HR;0.12MG/24HR
05 10.05MG/INH
06 10.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 10.1%
08 30.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 10.10MG/INH
10 10.11MG/INH
11 10.20MG/INH
12 10.22MG/INH
13 1100MG
14 210MG
15 110MG;100MG
16 110MG;10MG
17 110MG;20MG
18 110MG;40MG
19 110MG;80MG
20 112.5MG;100MG
21 112.5MG;50MG
22 215MG
23 11MG
24 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 12.5MG;120MG
26 120MG
27 1250MCG/0.5ML
28 125MG
29 225MG;100MG
30 125MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 125MG;250MG
32 230MG
33 13MG/ML;EQ 3MG BASE/ML
34 140MG
35 145MG
36 145MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
37 150MG
38 150MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
39 35MG
40 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
41 15MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
42 268MG/IMPLANT
43 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
44 1EQ 0.05% BASE
45 2EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 1EQ 0.05% BASE;1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
47 3EQ 10MG BASE
48 1EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
49 1EQ 10MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 1EQ 2% BASE
51 1EQ 20MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
52 1EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
53 1EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
54 1EQ 40MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
55 1EQ 4MG BASE
56 1EQ 4MG BASE/PACKET
57 1EQ 5MG BASE
58 3EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
59 1EQ 70MG BASE
60 1EQ 70MG BASE;2,800 IU
61 1EQ 70MG BASE;5,600 IU
62 1EQ 80MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 26DISCN
02 50RX
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FOSAMAX
Dosage Strength : EQ 10MG BASE **Federal R...
Approval Date : 1995-09-29
Application Number : 20560
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FOSAMAX
Dosage Strength : EQ 40MG BASE **Federal R...
Approval Date : 1995-09-29
Application Number : 20560
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FOSAMAX
Dosage Strength : EQ 5MG BASE **Federal Re...
Approval Date : 1997-04-25
Application Number : 20560
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FOSAMAX
Dosage Strength : EQ 35MG BASE **Federal R...
Approval Date : 2000-10-20
Application Number : 20560
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FOSAMAX
Dosage Strength : EQ 70MG BASE
Approval Date : 2000-10-20
Application Number : 20560
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
ALENDRONATE SODIUM; CHOLECALCIFEROL
Dosage Form : TABLET; ORAL
Proprietary Name : FOSAMAX PLUS D
Dosage Strength : EQ 70MG BASE;2,800 IU
Approval Date : 2005-04-07
Application Number : 21762
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ALENDRONATE SODIUM; CHOLECALCIFEROL
Dosage Form : TABLET; ORAL
Proprietary Name : FOSAMAX PLUS D
Dosage Strength : EQ 70MG BASE;5,600 IU
Approval Date : 2007-04-26
Application Number : 21762
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ATORVASTATIN CALCIUM; EZETIMIBE
Dosage Form : TABLET; ORAL
Proprietary Name : LIPTRUZET
Dosage Strength : EQ 10MG BASE;10MG **Fede...
Approval Date : 2013-05-03
Application Number : 200153
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ATORVASTATIN CALCIUM; EZETIMIBE
Dosage Form : TABLET; ORAL
Proprietary Name : LIPTRUZET
Dosage Strength : EQ 20MG BASE;10MG **Fede...
Approval Date : 2013-05-03
Application Number : 200153
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ATORVASTATIN CALCIUM; EZETIMIBE
Dosage Form : TABLET; ORAL
Proprietary Name : LIPTRUZET
Dosage Strength : EQ 40MG BASE;10MG **Fede...
Approval Date : 2013-05-03
Application Number : 200153
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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