01 3CABOZANTINIB
02 1CETRORELIX ACETATE
03 4ELTROMBOPAG CHOLINE
04 1HYDROCORTISONE
05 1MESALAMINE
06 1PACLITAXEL
07 1PAZOPANIB HYDROCHLORIDE
08 1TADALAFIL
09 2THEOPHYLLINE
10 2TIOPRONIN
11 2VALBENAZINE TOSYLATE
01 2CAPSULE;ORAL
02 1LOTION;TOPICAL
03 1POWDER;INTRAVENOUS
04 1POWDER;SUBCUTANEOUS
05 3TABLET, DELAYED RELEASE;ORAL
06 2TABLET, EXTENDED RELEASE;ORAL
07 9TABLET;ORAL
01 11%
02 1100MG
03 1100MG/VIAL
04 220MG
05 2300MG
06 240MG
07 1450MG
08 160MG
09 1800MG
10 180MG
11 1EQ 0.25MG BASE/VIAL
12 1EQ 18MG BASE
13 1EQ 200MG BASE
14 1EQ 36MG BASE
15 1EQ 54MG BASE
16 1EQ 9MG BASE
01 1DISCN
02 13RX
03 5Blank
RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CABOZANTINIB
Dosage Strength : 20MG
Approval Date :
Application Number : 215942
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CABOZANTINIB
Dosage Strength : 40MG
Approval Date :
Application Number : 215942
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CABOZANTINIB
Dosage Strength : 60MG
Approval Date :
Application Number : 215942
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code : AP
Dosage Form : POWDER; SUBCUTANEOUS
Proprietary Name : CETRORELIX ACETATE
Dosage Strength : EQ 0.25MG BASE/VIAL
Approval Date : 2022-08-12
Application Number : 215737
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALVAIZ
Dosage Strength : EQ 9MG BASE
Approval Date : 2023-11-29
Application Number : 216774
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALVAIZ
Dosage Strength : EQ 18MG BASE
Approval Date : 2023-11-29
Application Number : 216774
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALVAIZ
Dosage Strength : EQ 36MG BASE
Approval Date : 2023-11-29
Application Number : 216774
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALVAIZ
Dosage Strength : EQ 54MG BASE
Approval Date : 2023-11-29
Application Number : 216774
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : LOTION; TOPICAL
Proprietary Name : ACTICORT
Dosage Strength : 1%
Approval Date : 1982-01-01
Application Number : 86535
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : MESALAMINE
Dosage Strength : 800MG
Approval Date : 2024-08-22
Application Number : 213191
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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