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01 2ACETAZOLAMIDE
02 2AMINOCAPROIC ACID
03 3BACLOFEN
04 3BUMETANIDE
05 5CHLORPROMAZINE HYDROCHLORIDE
06 2CHLORTHALIDONE
07 1CLINDAMYCIN PALMITATE HYDROCHLORIDE
08 1CLOMIPHENE CITRATE
09 1CYPROHEPTADINE HYDROCHLORIDE
10 5DOXEPIN HYDROCHLORIDE
11 2FLUOXETINE HYDROCHLORIDE
12 2GLYCOPYRROLATE
13 6HALOPERIDOL
14 4HYDROXYCHLOROQUINE SULFATE
15 3IRBESARTAN
16 4LABETALOL HYDROCHLORIDE
17 2METRONIDAZOLE
18 2MODAFINIL
19 1NITROFURANTOIN
20 4PERPHENAZINE
21 3PRAZOSIN HYDROCHLORIDE
22 2RANITIDINE HYDROCHLORIDE
23 3SERTRALINE HYDROCHLORIDE
24 3SILDENAFIL CITRATE
25 1VALGANCICLOVIR HYDROCHLORIDE
26 2VENLAFAXINE HYDROCHLORIDE
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01 69APPCO
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01 10CAPSULE;ORAL
02 2FOR SOLUTION;ORAL
03 1SUSPENSION;ORAL
04 2TABLET, EXTENDED RELEASE;ORAL
05 54TABLET;ORAL
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01 20.5MG
02 4100MG
03 310MG
04 1125MG
05 1150MG
06 116MG
07 11GM
08 31MG
09 4200MG
10 220MG
11 2250MG
12 225MG
13 125MG/5ML
14 42MG
15 3300MG
16 2400MG
17 24MG
18 2500MG
19 350MG
20 150MG/ML
21 25MG
22 175MG
23 18MG
24 3EQ 100MG BASE
25 2EQ 10MG BASE
26 2EQ 150MG BASE
27 1EQ 1MG BASE
28 1EQ 20MG BASE
29 1EQ 225MG BASE
30 3EQ 25MG BASE
31 1EQ 2MG BASE
32 1EQ 300MG BASE
33 3EQ 50MG BASE
34 1EQ 5MG BASE
35 1EQ 75MG BASE
36 1EQ 75MG BASE/5ML
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01 69USA
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