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01 1DR REDDYS

02 2BRECKENRIDGE

03 2APOTEX

04 1EUGIA PHARMA

05 3MSN PHARMACEUTICALS INC

06 3ONYX PHARMS AMGEN

07 1QILU PHARM CO LTD

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

RLD : No

TE Code : AP

CARFILZOMIB

Brand Name : CARFILZOMIB

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : 60MG/VIAL

Approval Date : 2019-09-09

Application Number : 209422

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

Dr Reddy Company Banner

02

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AAPS 2024
Not Confirmed

CARFILZOMIB

Brand Name : CARFILZOMIB

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : 10MG/VIAL

Approval Date : 2021-06-11

Application Number : 209330

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Breckenridge Pharmaceutical

03

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AAPS 2024
Not Confirmed

CARFILZOMIB

Brand Name : CARFILZOMIB

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : 60MG/VIAL

Approval Date : 2021-06-11

Application Number : 209330

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Breckenridge Pharmaceutical

04

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

CARFILZOMIB

Brand Name : CARFILZOMIB

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : 60MG/VIAL

Approval Date : 2020-03-16

Application Number : 209425

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

AAPS 2024
Not Confirmed
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06

AAPS 2024
Not Confirmed
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07

AAPS 2024
Not Confirmed
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08

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

CARFILZOMIB

Brand Name : KYPROLIS

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : 60MG/VIAL

Approval Date : 2012-07-20

Application Number : 202714

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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09

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

CARFILZOMIB

Brand Name : KYPROLIS

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : 30MG/VIAL

Approval Date : 2016-06-03

Application Number : 202714

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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10

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

CARFILZOMIB

Brand Name : KYPROLIS

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : 10MG/VIAL

Approval Date : 2018-06-07

Application Number : 202714

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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