01 1AMINOCAPROIC ACID
02 3APREMILAST
03 4BRIVARACETAM
04 5BUPROPION 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 1LEVONORGESTREL
30 5LURASIDONE HYDROCHLORIDE
31 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
32 3MESALAMINE
33 1METFORMIN HYDROCHLORIDE
34 3MEXILETINE HYDROCHLORIDE
35 4MIRTAZAPINE
36 2NABUMETONE
37 1NIMODIPINE
38 1NITAZOXANIDE
39 1NITROFURANTOIN
40 3OXCARBAZEPINE
41 1PANTOPRAZOLE SODIUM
42 3PIOGLITAZONE HYDROCHLORIDE
43 1PITOLISANT
44 2POLYETHYLENE GLYCOL 3350
45 2PROMETHAZINE HYDROCHLORIDE
46 2PRUCALOPRIDE SUCCINATE
47 3SAPROPTERIN DIHYDROCHLORIDE
48 2SOLIFENACIN SUCCINATE
49 3SPIRONOLACTONE
50 2THEOPHYLLINE
51 2TOFACITINIB
52 3VENLAFAXINE HYDROCHLORIDE
53 1VIGABATRIN
54 2ZAFIRLUKAST
55 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 10TABLET, EXTENDED RELEASE;ORAL
16 4TABLET; ORAL
17 55TABLET;ORAL
01 10.25GM/ML
02 10.6MG
03 11.1G/ML
04 11.2GM
05 11.5MG
06 11.6GM/BOT;3.13GM/BOT;17.5GM/BOT
07 6100MG
08 1100MG/5ML
09 1100MG/PACKET
10 1100mg
11 710MG
12 110MG/ML
13 110MG; 5MG
14 112.5MG
15 1120MG
16 5150MG
17 115MG
18 117.8MG
19 117GM/PACKET
20 117GM/SCOOPFUL
21 2180MG
22 11GM
23 11MG/5ML
24 11MG/ML
25 3200MG
26 620MG
27 1250MG
28 1250MG/5ML
29 425MG
30 125MG/5ML
31 125MG; 5MG
32 125mg
33 5300MG
34 230MG
35 2360MG
36 1375MG
37 13MG/ML
38 240MG
39 140MG/5ML
40 1450MG
41 145MG
42 2500MG
43 1500MG/5ML
44 2500MG/PACKET
45 450MG
46 150mg
47 25MG
48 4600MG
49 160MG
50 166%;10%
51 17.5MG
52 1750MG
53 175mg
54 1800MG
55 180MG
56 290MG
57 1EQ 12.5MG ACID/PACKET
58 1EQ 150MG BASE
59 1EQ 15MG BASE
60 1EQ 1MG BASE
61 1EQ 20MG BASE
62 1EQ 250MG VALPROIC ACID
63 1EQ 25MG ACID/PACKET
64 1EQ 2MG BASE
65 1EQ 30MG BASE
66 1EQ 37.5MG BASE
67 2EQ 40MG BASE
68 1EQ 45MG BASE
69 1EQ 500MG VALPROIC ACID
70 1EQ 5MG BASE
71 1EQ 7.5MG BASE
72 1EQ 75MG BASE
01 6OTC
02 98RX
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 : AB3
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 150MG
Approval Date : 2025-10-01
Application Number : 217898
RX/OTC/DISCN : RX
RLD : No
TE Code : AB3
RLD : No
TE Code : AB3
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 300MG
Approval Date : 2025-10-01
Application Number : 217898
RX/OTC/DISCN : RX
RLD : No
TE Code : AB3
