01 3CONCIZUMAB
02 3CONCIZUMAB-MTCI
03 5ESTRADIOL
04 2ESTRADIOL; NORETHINDRONE ACETATE
05 2GLUCAGON HYDROCHLORIDE
06 3INSULIN ASPART
07 5INSULIN ASPART PROTAMINE RECOMBINANT; INSULIN ASPART RECOMBINANT
08 5INSULIN ASPART RECOMBINANT
09 1INSULIN ASPART; INSULIN DEGLUDEC
10 3INSULIN DEGLUDEC
11 1INSULIN DEGLUDEC; LIRAGLUTIDE
12 1INSULIN DETEMIR
13 5INSULIN DETEMIR RECOMBINANT
14 1INSULIN ICODEC
15 1INSULIN RECOMBINANT HUMAN
16 1INSULIN RECOMBINANT HUMAN; INSULIN SUSP ISOPHANE RECOMBINANT HUMAN
17 1INSULIN SUSP ISOPHANE RECOMBINANT HUMAN
18 2LIRAGLUTIDE
19 2METFORMIN HYDROCHLORIDE; REPAGLINIDE
20 3NEDOSIRAN SODIUM
21 22SEMAGLUTIDE
22 1SOMAPACITAN-BECO
23 11SOMATROPIN
01 1INJECTABLE; INJECTION
02 14INJECTABLE;INJECTION
03 15INJECTABLE;SUBCUTANEOUS
04 1INJECTION;SOLUTION
05 3Injectable; Subcutaneous
06 1POWDER;INTRAMUSCULAR, INTRAVENOUS
07 1POWDER;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
08 3SOLUTION; INJECTION
09 3SOLUTION;INJECTION
10 1SOLUTION;INTRAVENOUS, SUBCUTANEOUS
11 20SOLUTION;SUBCUTANEOUS
12 2TABLET; ORAL
13 17TABLET;ORAL
14 2TABLET;VAGINAL
01 10.25MG/0.5ML (0.25MG/0.5ML)
02 10.5MG
03 10.5MG/0.5ML (0.5MG/0.5ML)
04 21.5MG
05 11.7MG/0.75ML (1.7MG/0.75ML)
06 3100 UNITS/ML
07 41000 UNITS/10ML (100 UNITS/ML)
08 110MCG
09 410MG/1.5ML
10 114MG
11 1150MG/1.5ML (100MG/ML)
12 1150MG/1.5ML(100MG/ML)
13 315MG/1.5ML
14 218MG/3ML (6MG/ML)
15 11MG
16 21MG/0.5MG
17 11MG/0.5ML (1MG/0.5ML)
18 12.4MG/0.75ML (2.4MG/0.75ML)
19 1210 UNITS/3ML; 90 UNITS/3ML (70 UNITS/ML; 30 UNITS/ML)
20 2210 UNITS/3ML;90 UNITS/3ML (70 UNITS/ML; 30 UNITS/ML)
21 125MCG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 125MG
23 12MG
24 12MG/1.5ML (1.34MG/ML)
25 12MG/3ML (0.68MG/ML)
26 130 UNITS/ML;70 UNITS/ML
27 11300 UNITS/3ML (100 UNITS/ML)
28 1300 UNITS/3ML;10.8MG/3ML (100 UNITS/ML;3.6MG/ML)
29 1300MG/3ML (100MG/ML)
30 1300MG/3ML(100MG/ML)
31 230MG/3ML
32 23MG
33 24MG
34 14MG/3ML (1.34MG/ML)
35 150 UNITS/ML;50 UNITS/ML
36 1500MG;1MG
37 1500MG;2MG
38 35MG/1.5ML
39 1600 UNITS/3ML (200 UNITS/ML)
40 160MG/1.5ML (40MG/ML)
41 160MG/1.5ML(40MG/ML)
42 17.2MG/0.75ML (7.2MG/0.75ML)
43 1700 UNITS/10ML; 300 UNITS/10ML (70 UNITS/ML; 30 UNITS/ML)
44 27MG
45 18MG/3ML (2.68MG/ML)
46 190 UNITS/3ML;210 UNITS/3ML (30 UNITS/ML;70 UNITS/ML)
47 29MG
48 1EQ 128MG BASE/0.8ML (EQ 160MG BASE/ML)
49 1EQ 160MG BASE/ML (EQ 160MG BASE/ML)
50 2EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
51 1EQ 80MG BASE/0.5ML (EQ 160MG BASE/ML)
52 1Blank
01 9DISCN
02 25RX
03 50Blank
RLD :
TE Code :
Dosage Form : SOLUTION; INJECTION
Proprietary Name : ALHEMO
Dosage Strength : 60MG/1.5ML (40MG/ML)
Approval Date :
Application Number : 761428
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : SOLUTION; INJECTION
Proprietary Name : ALHEMO
Dosage Strength : 150MG/1.5ML (100MG/ML)
Approval Date :
Application Number : 761428
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : SOLUTION; INJECTION
Proprietary Name : ALHEMO
Dosage Strength : 300MG/3ML (100MG/ML)
Approval Date :
Application Number : 761428
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : Injectable; Subcutaneous
Proprietary Name : ALHEMO
Dosage Strength : 60MG/1.5ML(40MG/ML)
Approval Date :
Application Number : 761315
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : Injectable; Subcutaneous
Proprietary Name : ALHEMO
Dosage Strength : 150MG/1.5ML(100MG/ML)
Approval Date :
Application Number : 761315
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : Injectable; Subcutaneous
Proprietary Name : ALHEMO
Dosage Strength : 300MG/3ML(100MG/ML)
Approval Date :
Application Number : 761315
RX/OTC/DISCN :
RLD :
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; VAGINAL
Proprietary Name : VAGIFEM
Dosage Strength : 25MCG **Federal Register...
Approval Date : 1999-03-26
Application Number : 20908
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; VAGINAL
Proprietary Name : VAGIFEM
Dosage Strength : 10MCG
Approval Date : 2009-11-25
Application Number : 20908
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : INNOFEM
Dosage Strength : 0.5MG
Approval Date : 1999-11-19
Application Number : 40312
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : INNOFEM
Dosage Strength : 1MG
Approval Date : 1999-11-19
Application Number : 40312
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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