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 2POLYETHYLENE GLYCOL 3350
42 2PROMETHAZINE HYDROCHLORIDE
43 2PRUCALOPRIDE SUCCINATE
44 3SAPROPTERIN DIHYDROCHLORIDE
45 2SOLIFENACIN SUCCINATE
46 3SPIRONOLACTONE
47 2THEOPHYLLINE
48 2TOFACITINIB
49 3VENLAFAXINE HYDROCHLORIDE
50 1VIGABATRIN
51 2ZAFIRLUKAST
52 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 2TABLET
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 117GM/PACKET
17 117GM/SCOOPFUL
18 2180MG
19 11GM
20 11MG/5ML
21 11MG/ML
22 3200MG
23 620MG
24 1250MG
25 1250MG/5ML
26 425MG
27 125MG/5ML
28 125MG; 5MG
29 125mg
30 4300MG
31 130MG
32 2360MG
33 1375MG
34 13MG/ML
35 240MG
36 140MG/5ML
37 1450MG
38 2500MG
39 1500MG/5ML
40 2500MG/PACKET
41 450MG
42 150mg
43 25MG
44 4600MG
45 160MG
46 166%;10%
47 1750MG
48 175mg
49 1800MG
50 180MG
51 290MG
52 1EQ 12.5MG ACID/PACKET
53 1EQ 150MG BASE
54 1EQ 15MG BASE
55 1EQ 1MG BASE
56 1EQ 20MG BASE
57 1EQ 250MG VALPROIC ACID
58 1EQ 25MG ACID/PACKET
59 1EQ 2MG BASE
60 1EQ 30MG BASE
61 1EQ 37.5MG BASE
62 2EQ 40MG BASE
63 1EQ 45MG BASE
64 1EQ 500MG VALPROIC ACID
65 1EQ 5MG BASE
66 1EQ 7.5MG BASE
67 1EQ 75MG BASE
01 4OTC
02 91RX
03 13Blank
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
