01 2ABIRATERONE ACETATE
02 6LENALIDOMIDE
03 3MIDODRINE HYDROCHLORIDE
04 1PAZOPANIB HYDROCHLORIDE
05 2TRAMETINIB DIMETHYL SULFOXIDE
01 6CAPSULE;ORAL
02 8TABLET;ORAL
01 210MG
02 115MG
03 22.5MG
04 120MG
05 1250MG
06 125MG
07 1500MG
08 25MG
09 1EQ 0.5MG
10 1EQ 200MG BASE
11 1EQ 2MG
01 2DISCN
02 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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