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01 1FOSAPREPITANT DIMEGLUMINE
02 3LEVOTHYROXINE SODIUM
03 1METHYLENE BLUE
04 1ROCURONIUM BROMIDE
05 1SODIUM BICARBONATE
06 1SUCCINYLCHOLINE CHLORIDE
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01 2INJECTABLE;INJECTION
02 3POWDER;INTRAVENOUS
03 1SOLUTION;INTRAMUSCULAR, INTRAVENOUS
04 2SOLUTION;INTRAVENOUS
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01 1100MCG/VIAL
02 1100MG/5ML (20MG/ML)
03 11MEQ/ML
04 1200MCG/VIAL
05 1500MCG/VIAL
06 150MG/10ML (5MG/ML)
07 150MG/5ML (10MG/ML)
08 1EQ 150MG BASE/50ML (EQ 3MG BASE/ML)
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01 8RX
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 : POWDER; INTRAVENOUS
Proprietary Name : LEVOTHYROXINE SODIUM
Dosage Strength : 100MCG/VIAL
Approval Date : 2025-03-05
Application Number : 216729
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : LEVOTHYROXINE SODIUM
Dosage Strength : 200MCG/VIAL
Approval Date : 2025-03-05
Application Number : 216729
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : LEVOTHYROXINE SODIUM
Dosage Strength : 500MCG/VIAL
Approval Date : 2025-03-05
Application Number : 216729
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
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