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01 1AMINOCAPROIC ACID
02 1APOMORPHINE HYDROCHLORIDE
03 1BETAMETHASONE DIPROPIONATE
04 2BISOPROLOL FUMARATE
05 3CLOMIPRAMINE HYDROCHLORIDE
06 3CLONIDINE HYDROCHLORIDE
07 1CLOTRIMAZOLE
08 2DAPSONE
09 1FLUOCINOLONE ACETONIDE
10 1KETOCONAZOLE
11 1METHYLERGONOVINE MALEATE
12 2NAPROXEN
13 3OXAZEPAM
14 1OXYBUTYNIN CHLORIDE
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01 23TRUPHARMA
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01 6CAPSULE;ORAL
02 1CREAM;TOPICAL
03 2GEL;TOPICAL
04 1INJECTABLE;SUBCUTANEOUS
05 1OIL/DROPS;OTIC
06 1OINTMENT;TOPICAL
07 1SOLUTION;ORAL
08 1SOLUTION;TOPICAL
09 2TABLET, DELAYED RELEASE;ORAL
10 7TABLET;ORAL
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01 10.01%
02 10.1MG
03 10.25GM/ML
04 20.2MG
05 10.3MG
06 11%
07 210MG
08 115MG
09 12%
10 125MG
11 130MG
12 130MG/3ML (10MG/ML)
13 1375MG
14 15%
15 1500MG
16 150MG
17 25MG
18 17.5%
19 175MG
20 1EQ 0.05% BASE
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01 23USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : AMINOCAPROIC ACID
Dosage Strength : 0.25GM/ML
Packaging :
Approval Date : 2020-08-11
Application Number : 212494
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;SUBCUTANEOUS
Brand Name : APOMORPHINE HYDROCHLORIDE
Dosage Strength : 30MG/3ML (10MG/ML)
Packaging :
Approval Date : 2022-02-23
Application Number : 212025
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : BETAMETHASONE DIPROPIONAT...
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 2022-02-18
Application Number : 215186
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BISOPROLOL FUMARATE
Dosage Strength : 5MG
Packaging :
Approval Date : 2002-10-25
Application Number : 75474
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BISOPROLOL FUMARATE
Dosage Strength : 10MG
Packaging :
Approval Date : 2002-10-25
Application Number : 75474
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : CLOMIPRAMINE HYDROCHLORID...
Dosage Strength : 25MG
Packaging :
Approval Date : 2020-04-03
Application Number : 210653
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : CLOMIPRAMINE HYDROCHLORID...
Dosage Strength : 50MG
Packaging :
Approval Date : 2020-04-03
Application Number : 210653
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : CLOMIPRAMINE HYDROCHLORID...
Dosage Strength : 75MG
Packaging :
Approval Date : 2020-04-03
Application Number : 210653
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Strength : 0.3MG
Packaging :
Approval Date : 1987-09-04
Application Number : 70923
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Strength : 0.2MG
Packaging :
Approval Date : 1987-09-04
Application Number : 70923
Regulatory Info : RX
Registration Country : USA