01 1FOSAPREPITANT DIMEGLUMINE
02 1METHYLENE BLUE
03 1ROCURONIUM BROMIDE
04 1SODIUM BICARBONATE
05 1SUCCINYLCHOLINE CHLORIDE
06 9VANCOMYCIN HYDROCHLORIDE
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05 1EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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08 2EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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10 2EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 9DISCN
02 5RX
RLD : Yes
TE Code :
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : FOCINVEZ
Dosage Strength : EQ 150MG BASE/50ML (EQ 3...
Approval Date : 2023-08-22
Application Number : 216686
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code : AP
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : METHYLENE BLUE
Dosage Strength : 50MG/10ML (5MG/ML)
Approval Date : 2024-11-22
Application Number : 216955
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : ROCURONIUM BROMIDE
Dosage Strength : 50MG/5ML (10MG/ML)
Approval Date : 2024-07-22
Application Number : 217092
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : SODIUM BICARBONATE
Dosage Strength : 1MEQ/ML
Approval Date : 2023-06-28
Application Number : 217594
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Dosage Form : SOLUTION; INTRAMUSCULAR, INTRA...
Proprietary Name : SUCCINYLCHOLINE CHLORIDE
Dosage Strength : 100MG/5ML (20MG/ML)
Approval Date : 2024-07-09
Application Number : 217873
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 500MG BASE/VIAL
Approval Date : 1984-03-15
Application Number : 62476
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 1GM BASE/VIAL
Approval Date : 1986-03-21
Application Number : 62476
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 500MG BASE/VIAL
Approval Date : 1987-03-13
Application Number : 62716
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 1GM BASE/VIAL
Approval Date : 1987-03-13
Application Number : 62716
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : VANCOCIN HYDROCHLORIDE
Dosage Strength : EQ 500MG BASE/VIAL **Fed...
Approval Date : 1987-11-17
Application Number : 62812
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
