01 1FOSAPREPITANT DIMEGLUMINE
02 1METHYLENE BLUE
03 1ROCURONIUM BROMIDE
04 2SELENIOUS ACID
05 1SODIUM BICARBONATE
06 1SUCCINYLCHOLINE CHLORIDE
07 9VANCOMYCIN HYDROCHLORIDE
08 1ZIPRASIDONE MESYLATE
01 11INJECTABLE;INJECTION
02 2INJECTION;SOLUTION
03 1POWDER;INTRAMUSCULAR
04 1SOLUTION;INTRAMUSCULAR, INTRAVENOUS
05 2SOLUTION;INTRAVENOUS
01 1100MG/5ML (20MG/ML)
02 112UG/2ML
03 11MEQ/ML
04 150MG/10ML (5MG/ML)
05 150MG/5ML (10MG/ML)
06 160UG/1ML
07 1EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 1EQ 150MG BASE/50ML (EQ 3MG BASE/ML)
09 2EQ 1GM BASE/VIAL
10 2EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 1EQ 20MG BASE/VIAL
12 2EQ 500MG BASE/VIAL
13 2EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 9DISCN
02 6RX
03 2Blank
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 :
TE Code :
Dosage Form : INJECTION; SOLUTION
Proprietary Name : SELENIOUS ACID
Dosage Strength : 12UG/2ML
Approval Date :
Application Number : 219492
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : INJECTION; SOLUTION
Proprietary Name : SELENIOUS ACID
Dosage Strength : 60UG/1ML
Approval Date :
Application Number : 219492
RX/OTC/DISCN :
RLD :
TE Code :
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 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 :
