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01 3AVELUMAB
02 1CETRORELIX (CETRORELIX ACETATE)
03 2CETRORELIX ACETATE
04 4CHORIOGONADOTROPIN ALFA
05 2CLADRIBINE
06 1CLOMIPHENE CITRATE
07 7FOLLITROPIN ALFA
08 12FOLLITROPIN ALFA/BETA
09 4INTERFERON BETA-1A
10 23LEVOTHYROXINE SODIUM
11 4LUTROPIN ALFA
12 7METFORMIN HYDROCHLORIDE
13 3MITOXANTRONE HYDROCHLORIDE
14 1PROGESTERONE
15 3SERMORELIN ACETATE
16 14SOMATROPIN
17 4SOMATROPIN RECOMBINANT
18 1TEPOTINIB (TEPOTINIB HYDROCHLORIDE)
19 1TEPOTINIB HYDROCHLORIDE
20 1WATER
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01 32EMD SERONO
02 27EMD SERONO INC
03 28EMD SERONO, A DIVISION OF EMD INC., CANADA
04 11MERCK KGAA
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01 1GEL
02 20INJECTABLE;INJECTION
03 1INJECTABLE;INTRAVENOUS
04 14INJECTABLE;SUBCUTANEOUS
05 6POWDER FOR SOLUTION
06 2POWDER;SUBCUTANEOUS
07 19SOLUTION
08 2TABLET
09 2TABLET, EXTENDED RELEASE;ORAL
10 31TABLET;ORAL
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01 10.025MG
02 10.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
03 10.05MG
04 10.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
05 10.075MG
06 10.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
07 10.088MG
08 10.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
09 10.112MG
10 10.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
11 10.125MG
12 10.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
13 10.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
14 10.15MG
15 10.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
16 10.175MG
17 10.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
18 10.1MG
19 10.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
20 20.25MG/VIAL
21 10.2MG
22 10.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
23 20.3MG
24 11,050 IU/VIAL
25 210MG
26 1132MCG/1.5ML
27 1150 IU/0.25ML
28 2150 IU/VIAL
29 1150UNIT/0.48ML
30 11GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 11ML/KIT
32 320MG/ML
33 1225MG
34 1225UNIT/0.72ML
35 122MCG/0.5ML
36 2250MCG/0.5ML
37 1300 IU/0.5ML
38 1300UNIT/0.48ML
39 1300UNIT/0.5ML
40 237.5 IU/VIAL
41 144MCG/0.5ML
42 1450 IU/0.75ML
43 1450 IU/VIAL
44 1450UNIT/0.72ML
45 1450UNIT/0.75ML
46 1450UNIT/1.44ML
47 34MG/VIAL
48 15.5MCG/VIAL
49 15.83MG/ML
50 2500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
51 150MG
52 15MG/KIT
53 45MG/VIAL
54 1625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
55 166MCG/1.5ML
56 16MG/0.5ML (6MG/0.5ML)
57 36MG/VIAL
58 275 IU/VIAL
59 2750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
60 175UNIT/VIAL
61 18%
62 38.8MG/VIAL
63 1850MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
64 28MG/ML
65 1900 IU/1.5ML
66 1900UNIT/1.44ML
67 1900UNIT/1.5ML
68 1EQ 0.05MG BASE/AMP **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
69 1EQ 0.25MG /0.5ML
70 1EQ 0.25MG BASE/VIAL
71 1EQ 0.5MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
72 1EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
73 1EQ 20MG BASE/10ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
74 1EQ 225MG BASE
75 1EQ 25MG BASE/12.5ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
76 1EQ 30MG BASE/15ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
77 1EQ 3MG BASE/VIAL
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01 28Canada
02 70USA
Regulatory Info :
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : BAVENCIO
Dosage Strength : 20MG/ML
Packaging :
Approval Date :
Application Number : 761049
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : BAVENCIO
Dosage Strength : 20MG/ML
Packaging :
Approval Date :
Application Number : 761078
Regulatory Info :
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : BAVENCIO
Dosage Strength : 20MG/ML
Packaging : 10ML VIAL
Approval Date :
Application Number : 2469723
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
CETRORELIX (CETRORELIX ACETATE)
Dosage Form : POWDER FOR SOLUTION
Brand Name : CETROTIDE
Dosage Strength : 0.25MG/VIAL
Packaging : 1ML
Approval Date :
Application Number : 2247766
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;SUBCUTANEOUS
Brand Name : CETROTIDE
Dosage Strength : EQ 0.25MG BASE/VIAL
Packaging :
Approval Date : 2000-08-11
Application Number : 21197
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : POWDER;SUBCUTANEOUS
Brand Name : CETROTIDE
Dosage Strength : EQ 3MG BASE/VIAL
Packaging :
Approval Date : 2000-08-11
Application Number : 21197
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : OVIDREL
Dosage Strength : 0.25MG/VIAL
Packaging :
Approval Date :
Application Number : 21149
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : INJECTABLE;SUBCUTANEOUS
Brand Name : OVIDREL
Dosage Strength : EQ 0.25MG /0.5ML
Packaging :
Approval Date :
Application Number : 21149
Regulatory Info :
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : OVIDREL
Dosage Strength : 250MCG/0.5ML
Packaging : 0.5ML
Approval Date :
Application Number : 2262088
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : OVIDREL
Dosage Strength : 250MCG/0.5ML
Packaging : 0.5ML/3ML
Approval Date :
Application Number : 2371588
Regulatory Info : Prescription
Registration Country : Canada