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01 2ABIRATERONE ACETATE
02 6LENALIDOMIDE
03 3MIDODRINE HYDROCHLORIDE
04 1PAZOPANIB HYDROCHLORIDE
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01 6CAPSULE;ORAL
02 6TABLET;ORAL
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01 210MG
02 115MG
03 22.5MG
04 120MG
05 1250MG
06 125MG
07 1500MG
08 25MG
09 1EQ 200MG BASE
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01 12RX
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ABIRATERONE ACETATE
Dosage Strength : 250MG
Approval Date : 2022-01-05
Application Number : 215947
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ABIRATERONE ACETATE
Dosage Strength : 500MG
Approval Date : 2022-01-05
Application Number : 215947
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LENALIDOMIDE
Dosage Strength : 2.5MG
Approval Date : 2024-09-11
Application Number : 217281
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LENALIDOMIDE
Dosage Strength : 5MG
Approval Date : 2024-09-11
Application Number : 217281
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LENALIDOMIDE
Dosage Strength : 10MG
Approval Date : 2024-09-11
Application Number : 217281
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LENALIDOMIDE
Dosage Strength : 15MG
Approval Date : 2024-09-11
Application Number : 217281
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LENALIDOMIDE
Dosage Strength : 20MG
Approval Date : 2024-09-11
Application Number : 217281
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LENALIDOMIDE
Dosage Strength : 25MG
Approval Date : 2024-09-11
Application Number : 217281
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MIDODRINE HYDROCHLORIDE
Dosage Strength : 2.5MG
Approval Date : 2023-10-17
Application Number : 211973
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MIDODRINE HYDROCHLORIDE
Dosage Strength : 5MG
Approval Date : 2023-10-17
Application Number : 211973
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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