01 1FOSAPREPITANT DIMEGLUMINE
02 1METHYLENE BLUE
03 1ROCURONIUM BROMIDE
04 1SODIUM BICARBONATE
05 1SUCCINYLCHOLINE CHLORIDE
06 9VANCOMYCIN HYDROCHLORIDE
01 14STERISCIENCE
01 11INJECTABLE;INJECTION
02 1SOLUTION;INTRAMUSCULAR, INTRAVENOUS
03 2SOLUTION;INTRAVENOUS
01 1100MG/5ML (20MG/ML)
02 11MEQ/ML
03 150MG/10ML (5MG/ML)
04 150MG/5ML (10MG/ML)
05 1EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 1EQ 150MG BASE/50ML (EQ 3MG BASE/ML)
07 2EQ 1GM BASE/VIAL
08 2EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 2EQ 500MG BASE/VIAL
10 2EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 14USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : FOCINVEZ
Dosage Strength : EQ 150MG BASE/50ML (EQ...
Packaging :
Approval Date : 2023-08-22
Application Number : 216686
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : METHYLENE BLUE
Dosage Strength : 50MG/10ML (5MG/ML)
Packaging :
Approval Date : 2024-11-22
Application Number : 216955
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : ROCURONIUM BROMIDE
Dosage Strength : 50MG/5ML (10MG/ML)
Packaging :
Approval Date : 2024-07-22
Application Number : 217092
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : SODIUM BICARBONATE
Dosage Strength : 1MEQ/ML
Packaging :
Approval Date : 2023-06-28
Application Number : 217594
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAMUSCULAR, ...
Brand Name : SUCCINYLCHOLINE CHLORIDE
Dosage Strength : 100MG/5ML (20MG/ML)
Packaging :
Approval Date : 2024-07-09
Application Number : 217873
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 1GM BASE/VIAL **Fed...
Packaging :
Approval Date : 1986-03-21
Application Number : 60180
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1984-03-15
Application Number : 62476
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1987-03-13
Application Number : 62716
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 500MG BASE/VIAL **F...
Packaging :
Approval Date : 1987-11-17
Application Number : 62812
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 10GM BASE/VIAL **Fe...
Packaging :
Approval Date : 1987-11-17
Application Number : 62812
Regulatory Info : DISCN
Registration Country : USA
