01 3AMINOCAPROIC ACID
02 2ETRAVIRINE
03 1FAMOTIDINE
04 2PRIMIDONE
01 8CARNEGIE
01 1FOR SUSPENSION;ORAL
02 1SOLUTION;ORAL
03 6TABLET;ORAL
01 10.25GM/ML
02 1100MG
03 11GM
04 1200MG
05 1250MG
06 140MG/5ML
07 1500MG
08 150MG
01 8USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMINOCAPROIC ACID
Dosage Strength : 500MG
Packaging :
Approval Date : 2021-02-12
Application Number : 213928
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 : 2021-02-12
Application Number : 213928
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : AMINOCAPROIC ACID
Dosage Strength : 0.25GM/ML
Packaging :
Approval Date : 2021-01-26
Application Number : 214140
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ETRAVIRINE
Dosage Strength : 100MG
Packaging :
Approval Date : 2022-04-13
Application Number : 215402
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ETRAVIRINE
Dosage Strength : 200MG
Packaging :
Approval Date : 2022-04-13
Application Number : 215402
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : FAMOTIDINE
Dosage Strength : 40MG/5ML
Packaging :
Approval Date : 2023-07-07
Application Number : 217137
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PRIMIDONE
Dosage Strength : 50MG
Packaging :
Approval Date : 2024-01-23
Application Number : 218366
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PRIMIDONE
Dosage Strength : 250MG
Packaging :
Approval Date : 2024-01-23
Application Number : 218366
Regulatory Info : RX
Registration Country : USA
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