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01 2ACETAZOLAMIDE
02 2AMINOCAPROIC ACID
03 3BACLOFEN
04 3BUMETANIDE
05 5CHLORPROMAZINE HYDROCHLORIDE
06 2CHLORTHALIDONE
07 2CHLORZOXAZONE
08 1CLINDAMYCIN PALMITATE HYDROCHLORIDE
09 1CLOMIPHENE CITRATE
10 1CYPROHEPTADINE HYDROCHLORIDE
11 4DOXAZOSIN MESYLATE
12 5DOXEPIN HYDROCHLORIDE
13 1FAMOTIDINE
14 2FLUOXETINE HYDROCHLORIDE
15 2GLYCOPYRROLATE
16 6HALOPERIDOL
17 4HYDROXYCHLOROQUINE SULFATE
18 3IRBESARTAN
19 4LABETALOL HYDROCHLORIDE
20 2LAMIVUDINE
21 2METRONIDAZOLE
22 2MODAFINIL
23 1NITROFURANTOIN
24 4PERPHENAZINE
25 3PRAZOSIN HYDROCHLORIDE
26 1RAMELTEON
27 2RANITIDINE HYDROCHLORIDE
28 3SERTRALINE HYDROCHLORIDE
29 3SILDENAFIL CITRATE
30 1VALGANCICLOVIR HYDROCHLORIDE
31 2VENLAFAXINE HYDROCHLORIDE
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01 79APPCO
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01 10CAPSULE;ORAL
02 2FOR SOLUTION;ORAL
03 1FOR SUSPENSION;ORAL
04 1SUSPENSION;ORAL
05 2TABLET, EXTENDED RELEASE;ORAL
06 63TABLET;ORAL
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01 20.5MG
02 4100MG
03 310MG
04 1125MG
05 2150MG
06 116MG
07 11GM
08 31MG
09 4200MG
10 220MG
11 2250MG
12 225MG
13 125MG/5ML
14 42MG
15 4300MG
16 1375MG
17 2400MG
18 140MG/5ML
19 24MG
20 2500MG
21 350MG
22 150MG/ML
23 25MG
24 1750MG
25 175MG
26 28MG
27 3EQ 100MG BASE
28 2EQ 10MG BASE
29 2EQ 150MG BASE
30 2EQ 1MG BASE
31 1EQ 20MG BASE
32 1EQ 225MG BASE
33 3EQ 25MG BASE
34 2EQ 2MG BASE
35 1EQ 300MG BASE
36 1EQ 4MG BASE
37 3EQ 50MG BASE
38 1EQ 5MG BASE
39 1EQ 75MG BASE
40 1EQ 75MG BASE/5ML
41 1EQ 8MG BASE
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01 79USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACETAZOLAMIDE
Dosage Strength : 125MG
Packaging :
Approval Date : 2021-02-22
Application Number : 211372
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACETAZOLAMIDE
Dosage Strength : 250MG
Packaging :
Approval Date : 2021-02-22
Application Number : 211372
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMINOCAPROIC ACID
Dosage Strength : 500MG
Packaging :
Approval Date : 2022-09-14
Application Number : 213944
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMINOCAPROIC ACID
Dosage Strength : 1GM
Packaging :
Approval Date : 2022-09-14
Application Number : 213944
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BACLOFEN
Dosage Strength : 10MG
Packaging :
Approval Date : 2010-02-18
Application Number : 90334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BACLOFEN
Dosage Strength : 20MG
Packaging :
Approval Date : 2010-02-18
Application Number : 90334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BACLOFEN
Dosage Strength : 5MG
Packaging :
Approval Date : 2025-01-31
Application Number : 90334
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUMETANIDE
Dosage Strength : 0.5MG
Packaging :
Approval Date : 2024-09-18
Application Number : 212931
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUMETANIDE
Dosage Strength : 1MG
Packaging :
Approval Date : 2024-09-18
Application Number : 212931
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUMETANIDE
Dosage Strength : 2MG
Packaging :
Approval Date : 2024-09-18
Application Number : 212931
Regulatory Info : RX
Registration Country : USA