01 1CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE
02 3FENOPROFEN CALCIUM
03 3KETOPROFEN
01 7MISEMER
01 7CAPSULE;ORAL
01 125MG
02 150MG
03 15MG;2.5MG
04 175MG
05 1EQ 200MG BASE
06 1EQ 300MG BASE
07 1EQ 400MG BASE
01 7USA
Regulatory Info : RX
Registration Country : USA
CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE
Dosage Form : CAPSULE;ORAL
Brand Name : CHLORDIAZEPOXIDE HYDROCHL...
Dosage Strength : 5MG;2.5MG
Packaging :
Approval Date : 2020-07-29
Application Number : 210579
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : FENOPROFEN CALCIUM
Dosage Strength : EQ 200MG BASE
Packaging :
Approval Date : 2023-05-16
Application Number : 215548
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : FENOPROFEN CALCIUM
Dosage Strength : EQ 300MG BASE
Packaging :
Approval Date : 2023-05-16
Application Number : 215548
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : FENOPROFEN CALCIUM
Dosage Strength : EQ 400MG BASE
Packaging :
Approval Date : 2023-05-16
Application Number : 215548
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : KETOPROFEN
Dosage Strength : 25MG
Packaging :
Approval Date : 1993-01-29
Application Number : 74014
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : KETOPROFEN
Dosage Strength : 50MG
Packaging :
Approval Date : 1993-01-29
Application Number : 74014
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : KETOPROFEN
Dosage Strength : 75MG
Packaging :
Approval Date : 1993-01-29
Application Number : 74014
Regulatory Info : RX
Registration Country : USA
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