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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 2ELTROMBOPAG OLAMINE
14 2EMPAGLIFLOZIN
15 2EMPAGLIFLOZIN;LINAGLIPTIN
16 1ENALAPRIL MALEATE
17 2EPLERENONE
18 5FAMOTIDINE
19 3GABAPENTIN
20 1GLYCEROL PHENYLBUTYRATE
21 1GLYCOPYRROLATE
22 1IBUPROFEN
23 1ITRACONAZOLE
24 2IVABRADINE HYDROCHLORIDE
25 1LAMIVUDINE
26 5LURASIDONE HYDROCHLORIDE
27 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
28 2MESALAMINE
29 1METFORMIN HYDROCHLORIDE
30 3MEXILETINE HYDROCHLORIDE
31 2NABUMETONE
32 1NIMODIPINE
33 3OXCARBAZEPINE
34 1PANTOPRAZOLE SODIUM
35 3PIOGLITAZONE HYDROCHLORIDE
36 1POLYETHYLENE GLYCOL 3350
37 2PROMETHAZINE HYDROCHLORIDE
38 3SAPROPTERIN DIHYDROCHLORIDE
39 2SOLIFENACIN SUCCINATE
40 2THEOPHYLLINE
41 3VENLAFAXINE HYDROCHLORIDE
42 1VIGABATRIN
43 2ZAFIRLUKAST
44 1ZILEUTON
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01 3CAPSULE, EXTENDED RELEASE;ORAL
02 8CAPSULE;ORAL
03 3FOR 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 3SUPPOSITORY;RECTAL
12 1SUSPENSION;ORAL
13 1TABLET, DELAYED RELEASE;ORAL
14 8TABLET, EXTENDED RELEASE;ORAL
15 4TABLET; ORAL
16 42TABLET;ORAL
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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 4100MG
07 1100MG/5ML
08 1100MG/PACKET
09 1100mg
10 610MG
11 110MG/ML
12 110MG; 5MG
13 112.5MG
14 1120MG
15 3150MG
16 117GM/SCOOPFUL
17 2180MG
18 11GM
19 11MG/5ML
20 11MG/ML
21 3200MG
22 620MG
23 1250MG
24 1250MG/5ML
25 325MG
26 125MG; 5MG
27 125mg
28 4300MG
29 130MG
30 2360MG
31 13MG/ML
32 240MG
33 140MG/5ML
34 1450MG
35 1500MG
36 1500MG/5ML
37 2500MG/PACKET
38 250MG
39 150mg
40 15MG
41 4600MG
42 160MG
43 166%;10%
44 1750MG
45 175mg
46 1800MG
47 180MG
48 290MG
49 1EQ 12.5MG ACID/PACKET
50 1EQ 150MG BASE
51 1EQ 15MG BASE
52 1EQ 250MG VALPROIC ACID
53 1EQ 25MG ACID/PACKET
54 1EQ 30MG BASE
55 1EQ 37.5MG BASE
56 1EQ 40MG BASE
57 1EQ 45MG BASE
58 1EQ 500MG VALPROIC ACID
59 1EQ 5MG BASE
60 1EQ 7.5MG BASE
61 1EQ 75MG BASE
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01 4OTC
02 78RX
03 10Blank
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