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 4DESLORATADINE
10 2DESLORATADINE; PSEUDOEPHEDRINE SULFATE
11 1ETHINYL ESTRADIOL; ETONOGESTREL
12 2ETONOGESTREL
13 1EZETIMIBE
14 4EZETIMIBE; SIMVASTATIN
15 2FINASTERIDE
16 4FOLLITROPIN ALFA/BETA
17 3FORMOTEROL FUMARATE; MOMETASONE FUROATE
18 1GANIRELIX ACETATE
19 1GONADOTROPIN, CHORIONIC
20 3HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
21 3LOSARTAN POTASSIUM
22 6MIRTAZAPINE
23 10MOMETASONE FUROATE
24 4MONTELUKAST SODIUM
25 4RIZATRIPTAN BENZOATE
26 5SIMVASTATIN
27 1TAPINAROF
01 6AEROSOL, METERED;INHALATION
02 1CREAM, AUGMENTED;TOPICAL
03 4CREAM;TOPICAL
04 1GEL;VAGINAL
05 1GRANULE;ORAL
06 2IMPLANT;IMPLANTATION
07 3INJECTABLE;INJECTION
08 4INJECTABLE;SUBCUTANEOUS
09 1LOTION, AUGMENTED;TOPICAL
10 1LOTION;TOPICAL
11 1OINTMENT, AUGMENTED;TOPICAL
12 1OINTMENT;TOPICAL
13 2POWDER;INHALATION
14 1RING;VAGINAL
15 1SOLUTION;ORAL
16 1SPRAY, METERED;NASAL
17 2TABLET, CHEWABLE;ORAL
18 4TABLET, EXTENDED RELEASE;ORAL
19 7TABLET, ORALLY DISINTEGRATING;ORAL
20 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06 10.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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08 30.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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13 10.5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 11%
15 110,000 UNITS/VIAL
16 1100MG
17 210MG
18 110MG;100MG
19 110MG;10MG
20 110MG;20MG
21 110MG;40MG
22 110MG;80MG
23 112.5MG;100MG
24 112.5MG;50MG
25 1150 IU/0.18ML
26 215MG
27 11MG
28 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 12.5MG;120MG
30 120MG
31 1250MCG/0.5ML
32 125MG
33 225MG;100MG
34 125MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 125MG;250MG
36 1300 IU/0.36ML
37 230MG
38 13MG/ML;EQ 3MG BASE/ML
39 140MG
40 145MG
41 145MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
42 150MG
43 150MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
44 35MG
45 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 15MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
47 1600 IU/0.72ML
48 268MG/IMPLANT
49 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 1900 IU/1.08ML
51 1EQ 0.05% BASE
52 2EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
53 1EQ 0.05% BASE;1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
54 3EQ 10MG BASE
55 1EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
56 1EQ 10MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
57 1EQ 2% BASE
58 1EQ 20MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
59 1EQ 35MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
60 1EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
61 1EQ 40MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 1EQ 4MG BASE
63 1EQ 4MG BASE/PACKET
64 1EQ 5MG BASE
65 3EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
66 1EQ 70MG BASE
67 1EQ 70MG BASE;2,800 IU
68 1EQ 70MG BASE;5,600 IU
69 1EQ 80MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 27DISCN
02 51RX
03 5Blank
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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