01 1AMINOCAPROIC ACID
02 3APREMILAST
03 4BRIVARACETAM
04 3BUPROPION HYDROCHLORIDE
05 1COLCHICINE
06 6DEFERASIROX
07 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM
08 1DICLOFENAC POTASSIUM
09 2DICYCLOMINE HYDROCHLORIDE
10 2DIVALPROEX SODIUM
11 3DROXIDOPA
12 2ELTROMBOPAG OLAMINE
13 2EMPAGLIFLOZIN
14 2EMPAGLIFLOZIN;LINAGLIPTIN
15 1ENALAPRIL MALEATE
16 2EPLERENONE
17 5FAMOTIDINE
18 3GABAPENTIN
19 1GLYCEROL PHENYLBUTYRATE
20 1GLYCOPYRROLATE
21 1IBUPROFEN
22 1ITRACONAZOLE
23 2IVABRADINE HYDROCHLORIDE
24 1LAMIVUDINE
25 5LURASIDONE HYDROCHLORIDE
26 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
27 2MESALAMINE
28 3MEXILETINE HYDROCHLORIDE
29 2NABUMETONE
30 1NIMODIPINE
31 3OXCARBAZEPINE
32 1PANTOPRAZOLE SODIUM
33 3PIOGLITAZONE HYDROCHLORIDE
34 1POLYETHYLENE GLYCOL 3350
35 2PROMETHAZINE HYDROCHLORIDE
36 3SAPROPTERIN DIHYDROCHLORIDE
37 2SOLIFENACIN SUCCINATE
38 2THEOPHYLLINE
39 3VENLAFAXINE HYDROCHLORIDE
40 1VIGABATRIN
41 2ZAFIRLUKAST
42 1ZILEUTON
01 7ANNORA
02 82ANNORA PHARMA
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 7SOLUTION;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 40TABLET;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 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 2500MG/PACKET
37 250MG
38 150mg
39 15MG
40 3600MG
41 160MG
42 166%;10%
43 1750MG
44 175mg
45 180MG
46 290MG
47 1EQ 12.5MG ACID/PACKET
48 1EQ 150MG BASE
49 1EQ 15MG BASE
50 1EQ 250MG VALPROIC ACID
51 1EQ 25MG ACID/PACKET
52 1EQ 30MG BASE
53 1EQ 37.5MG BASE
54 1EQ 40MG BASE
55 1EQ 45MG BASE
56 1EQ 500MG VALPROIC ACID
57 1EQ 5MG BASE
58 1EQ 7.5MG BASE
59 1EQ 75MG BASE
01 89USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : AMINOCAPROIC ACID
Dosage Strength : 0.25GM/ML
Packaging :
Approval Date : 2022-11-04
Application Number : 216464
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : APREMILAST
Dosage Strength : 10MG
Packaging :
Approval Date : 2023-07-26
Application Number : 211878
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : APREMILAST
Dosage Strength : 20MG
Packaging :
Approval Date : 2023-07-26
Application Number : 211878
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : APREMILAST
Dosage Strength : 30MG
Packaging :
Approval Date : 2023-07-26
Application Number : 211878
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET; ORAL
Brand Name : BRIVARACETAM
Dosage Strength : 25mg
Packaging :
Approval Date :
Application Number : 214831
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET; ORAL
Brand Name : BRIVARACETAM
Dosage Strength : 50mg
Packaging :
Approval Date :
Application Number : 214831
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET; ORAL
Brand Name : BRIVARACETAM
Dosage Strength : 75mg
Packaging :
Approval Date :
Application Number : 214831
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET; ORAL
Brand Name : BRIVARACETAM
Dosage Strength : 100mg
Packaging :
Approval Date :
Application Number : 214831
Regulatory Info :
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 100MG
Packaging :
Approval Date : 2023-05-31
Application Number : 216800
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 200MG
Packaging :
Approval Date : 2023-05-31
Application Number : 216800
Regulatory Info : RX
Registration Country : USA
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