01 3CLINDAMYCIN PHOSPHATE
02 1DOXORUBICIN HYDROCHLORIDE
03 1MELPHALAN HYDROCHLORIDE
04 1TERIPARATIDE
05 1VORICONAZOLE
01 7ALMAJECT
01 5INJECTABLE;INJECTION
02 1INJECTABLE;INTRAVENOUS
03 1SOLUTION;SUBCUTANEOUS
01 10.6MG/2.4ML (0.25MG/ML)
02 1200MG/VIAL
03 12MG/ML
04 3EQ 150MG BASE/ML
05 1EQ 50MG BASE/VIAL
01 7USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CLINDAMYCIN PHOSPHATE
Dosage Strength : EQ 150MG BASE/ML
Packaging :
Approval Date : 1987-07-24
Application Number : 62800
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CLINDAMYCIN PHOSPHATE
Dosage Strength : EQ 150MG BASE/ML
Packaging :
Approval Date : 1987-07-24
Application Number : 62801
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CLINDAMYCIN PHOSPHATE
Dosage Strength : EQ 150MG BASE/ML
Packaging :
Approval Date : 1988-09-29
Application Number : 62943
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : DOXORUBICIN HYDROCHLORIDE
Dosage Strength : 2MG/ML
Packaging :
Approval Date : 2012-11-08
Application Number : 65515
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : MELPHALAN HYDROCHLORIDE
Dosage Strength : EQ 50MG BASE/VIAL
Packaging :
Approval Date : 2019-05-17
Application Number : 204817
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : TERIPARATIDE
Dosage Strength : 0.6MG/2.4ML (0.25MG/ML...
Packaging :
Approval Date : 2024-06-04
Application Number : 218771
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : VORICONAZOLE
Dosage Strength : 200MG/VIAL
Packaging :
Approval Date : 2016-03-23
Application Number : 206398
Regulatory Info : RX
Registration Country : USA
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