01 2ACETAZOLAMIDE
02 2AMINOCAPROIC ACID
03 2BACLOFEN
04 3BUMETANIDE
05 5CHLORPROMAZINE HYDROCHLORIDE
06 2CHLORTHALIDONE
07 1CYPROHEPTADINE HYDROCHLORIDE
08 5DOXEPIN HYDROCHLORIDE
09 4HYDROXYCHLOROQUINE SULFATE
10 4LABETALOL HYDROCHLORIDE
11 2MODAFINIL
12 4PERPHENAZINE
13 3PRAZOSIN HYDROCHLORIDE
14 2RANITIDINE HYDROCHLORIDE
15 3SERTRALINE HYDROCHLORIDE
16 3SILDENAFIL CITRATE
17 1VALGANCICLOVIR HYDROCHLORIDE
18 2VENLAFAXINE HYDROCHLORIDE
01 50APPCO
01 10CAPSULE;ORAL
02 1FOR SOLUTION;ORAL
03 2TABLET, EXTENDED RELEASE;ORAL
04 37TABLET;ORAL
01 10.5MG
02 4100MG
03 210MG
04 1125MG
05 116MG
06 11GM
07 11MG
08 4200MG
09 120MG
10 1250MG
11 225MG
12 22MG
13 2300MG
14 2400MG
15 24MG
16 1500MG
17 250MG
18 150MG/ML
19 18MG
20 3EQ 100MG BASE
21 1EQ 10MG BASE
22 2EQ 150MG BASE
23 1EQ 1MG BASE
24 1EQ 225MG BASE
25 3EQ 25MG BASE
26 1EQ 2MG BASE
27 1EQ 300MG BASE
28 3EQ 50MG BASE
29 1EQ 5MG BASE
30 1EQ 75MG BASE
01 50USA
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 : 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
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CHLORPROMAZINE HYDROCHLOR...
Dosage Strength : 10MG
Packaging :
Approval Date : 2020-08-31
Application Number : 213590
Regulatory Info : RX
Registration Country : USA
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