01 1DOXYCYCLINE HYCLATE
02 1FOSAPREPITANT DIMEGLUMINE
03 1METHYLENE BLUE
04 1ROCURONIUM BROMIDE
05 1SELENIOUS ACID
06 1SODIUM BICARBONATE
07 1SUCCINYLCHOLINE CHLORIDE
08 12VANCOMYCIN HYDROCHLORIDE
09 1ZIPRASIDONE MESYLATE
01 11INJECTABLE;INJECTION
02 1INJECTION;SOLUTION
03 1POWDER;INTRAMUSCULAR
04 3POWDER;INTRAVENOUS
05 1SOLUTION;INTRAMUSCULAR, INTRAVENOUS
06 3SOLUTION;INTRAVENOUS
01 1100MG/5ML (20MG/ML)
02 150MEQ/50ML (1MEQ/ML)
03 150MG/10ML (5MG/ML)
04 150MG/5ML (10MG/ML)
05 1600MCG/10ML
06 1EQ 1.25GM BASE/VIAL
07 1EQ 1.5GM BASE/VIAL
08 1EQ 100MG BASE/VIAL
09 1EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1EQ 150MG BASE/50ML (EQ 3MG BASE/ML)
11 2EQ 1GM BASE/VIAL
12 2EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
13 1EQ 20MG BASE/VIAL
14 2EQ 500MG BASE/VIAL
15 2EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 1EQ 750MG BASE/VIAL
01 9DISCN
02 10RX
03 1Blank
RLD : No
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : DOXYCYCLINE HYCLATE
Dosage Strength : EQ 100MG BASE/VIAL
Approval Date : 2025-11-06
Application Number : 217972
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
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 : 600MCG/10ML
Approval Date :
Application Number : 219492
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code : AP
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : SODIUM BICARBONATE
Dosage Strength : 50MEQ/50ML (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 **Fed...
Approval Date : 1982-01-01
Application Number : 60180
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 **Feder...
Approval Date : 1986-03-21
Application Number : 60180
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 :
