01 1AMINOCAPROIC ACID
02 3APREMILAST
03 4BRIVARACETAM
04 3BUPROPION HYDROCHLORIDE
05 1COLCHICINE
06 2DARUNAVIR
07 6DEFERASIROX
08 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM
09 1DICLOFENAC POTASSIUM
10 2DICYCLOMINE HYDROCHLORIDE
11 2DIVALPROEX SODIUM
12 3DROXIDOPA
13 2ELETRIPTAN HYDROBROMIDE
14 2ELTROMBOPAG OLAMINE
15 2EMPAGLIFLOZIN
16 2EMPAGLIFLOZIN;LINAGLIPTIN
17 1ENALAPRIL MALEATE
18 2EPLERENONE
19 5FAMOTIDINE
20 2FLUVOXAMINE MALEATE
21 3GABAPENTIN
22 1GLYCEROL PHENYLBUTYRATE
23 1GLYCOPYRROLATE
24 1IBUPROFEN
25 1INDOMETHACIN
26 1ITRACONAZOLE
27 2IVABRADINE HYDROCHLORIDE
28 1LAMIVUDINE
29 5LURASIDONE HYDROCHLORIDE
30 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
31 3MESALAMINE
32 1METFORMIN HYDROCHLORIDE
33 3MEXILETINE HYDROCHLORIDE
34 2NABUMETONE
35 1NIMODIPINE
36 1NITAZOXANIDE
37 1NITROFURANTOIN
38 3OXCARBAZEPINE
39 1PANTOPRAZOLE SODIUM
40 3PIOGLITAZONE HYDROCHLORIDE
41 1PITOLISANT
42 2POLYETHYLENE GLYCOL 3350
43 2PROMETHAZINE HYDROCHLORIDE
44 2PRUCALOPRIDE SUCCINATE
45 3SAPROPTERIN DIHYDROCHLORIDE
46 2SOLIFENACIN SUCCINATE
47 3SPIRONOLACTONE
48 2THEOPHYLLINE
49 2TOFACITINIB
50 3VENLAFAXINE HYDROCHLORIDE
51 1VIGABATRIN
52 2ZAFIRLUKAST
53 1ZILEUTON
01 6CAPSULE, EXTENDED RELEASE;ORAL
02 8CAPSULE;ORAL
03 4FOR SOLUTION;ORAL
04 1FOR SUSPENSION, DELAYED RELEASE;ORAL
05 3FOR SUSPENSION;ORAL
06 3GRANULE;ORAL
07 1LIQUID;ORAL
08 2POWDER;ORAL
09 8SOLUTION;ORAL
10 1SOLUTION;ORAL, RECTAL
11 4SUPPOSITORY;RECTAL
12 2SUSPENSION;ORAL
13 3TABLET
14 1TABLET, DELAYED RELEASE;ORAL
15 8TABLET, EXTENDED RELEASE;ORAL
16 4TABLET; ORAL
17 50TABLET;ORAL
01 10.25GM/ML
02 10.6MG
03 11.1G/ML
04 11.2GM
05 11.6GM/BOT;3.13GM/BOT;17.5GM/BOT
06 6100MG
07 1100MG/5ML
08 1100MG/PACKET
09 1100mg
10 710MG
11 110MG/ML
12 110MG; 5MG
13 112.5MG
14 1120MG
15 4150MG
16 117.8MG
17 117GM/PACKET
18 117GM/SCOOPFUL
19 2180MG
20 11GM
21 11MG/5ML
22 11MG/ML
23 3200MG
24 620MG
25 1250MG
26 1250MG/5ML
27 425MG
28 125MG/5ML
29 125MG; 5MG
30 125mg
31 4300MG
32 130MG
33 2360MG
34 1375MG
35 13MG/ML
36 240MG
37 140MG/5ML
38 1450MG
39 2500MG
40 1500MG/5ML
41 2500MG/PACKET
42 450MG
43 150mg
44 25MG
45 4600MG
46 160MG
47 166%;10%
48 1750MG
49 175mg
50 1800MG
51 180MG
52 290MG
53 1EQ 12.5MG ACID/PACKET
54 1EQ 150MG BASE
55 1EQ 15MG BASE
56 1EQ 1MG BASE
57 1EQ 20MG BASE
58 1EQ 250MG VALPROIC ACID
59 1EQ 25MG ACID/PACKET
60 1EQ 2MG BASE
61 1EQ 30MG BASE
62 1EQ 37.5MG BASE
63 2EQ 40MG BASE
64 1EQ 45MG BASE
65 1EQ 500MG VALPROIC ACID
66 1EQ 5MG BASE
67 1EQ 7.5MG BASE
68 1EQ 75MG BASE
01 5OTC
02 92RX
03 12Blank
RLD : No
TE Code : AA
Dosage Form : SOLUTION; ORAL
Proprietary Name : AMINOCAPROIC ACID
Dosage Strength : 0.25GM/ML
Approval Date : 2022-11-04
Application Number : 216464
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : APREMILAST
Dosage Strength : 10MG
Approval Date : 2023-07-26
Application Number : 211878
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : APREMILAST
Dosage Strength : 20MG
Approval Date : 2023-07-26
Application Number : 211878
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : APREMILAST
Dosage Strength : 30MG
Approval Date : 2023-07-26
Application Number : 211878
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BRIVARACETAM
Dosage Strength : 25mg
Approval Date :
Application Number : 214831
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BRIVARACETAM
Dosage Strength : 50mg
Approval Date :
Application Number : 214831
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BRIVARACETAM
Dosage Strength : 75mg
Approval Date :
Application Number : 214831
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BRIVARACETAM
Dosage Strength : 100mg
Approval Date :
Application Number : 214831
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code : AB1
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 100MG
Approval Date : 2023-05-31
Application Number : 216800
RX/OTC/DISCN : RX
RLD : No
TE Code : AB1
RLD : No
TE Code : AB1
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 150MG
Approval Date : 2023-05-31
Application Number : 216800
RX/OTC/DISCN : RX
RLD : No
TE Code : AB1
