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Approved Drug Products containing NCGC00024415-33 listed in the FDA Orange Book. Original Data : FDA Website

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01 2DR REDDYS

02 2ACTAVIS INC

03 1ALMAJECT

04 2AMNEAL

05 2AYANA PHARMA LTD

06 4BAXTER HLTHCARE CORP

07 3BRISTOL MYERS SQUIBB

08 2FORDOZ

09 1FRESENIUS KABI USA

10 1GLAND PHARMA LTD

11 5HIKMA

12 1HISUN PHARM HANGZHOU

13 1HLTHCARE

14 2MYLAN LABS LTD

15 1NORVIUM BIOSCIENCE

16 9PFIZER

17 5PHARMACHEMIE BV

18 1SAGENT PHARMS

19 2SUN PHARM

20 1SUN PHARM INDS

21 2TEVA PHARMS USA

22 2ZYDUS LIFESCIENCES

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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 : AB

DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE (LIPOSOMAL)

Dosage Form : INJECTABLE, LIPOSOMAL;INJECTION

Dosage Strength : 20MG/10ML (2MG/ML)

Approval Date : 2017-05-15

Application Number : 208657

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code : AB

DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE (LIPOSOMAL)

Dosage Form : INJECTABLE, LIPOSOMAL;INJECTION

Dosage Strength : 50MG/25ML (2MG/ML)

Approval Date : 2017-05-15

Application Number : 208657

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

03

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DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXIL (LIPOSOMAL)

Dosage Form : INJECTABLE, LIPOSOMAL;INJECTION

Dosage Strength : 20MG/10ML (2MG/ML)

Approval Date : 1995-11-17

Application Number : 50718

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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04

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DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/VIAL

Approval Date : 1982-01-01

Application Number : 50467

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

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DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/VIAL

Approval Date : 1982-01-01

Application Number : 50467

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

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DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/VIAL

Approval Date : 1985-05-20

Application Number : 50467

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

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DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 150MG/VIAL

Approval Date : 1987-07-22

Application Number : 50467

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

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DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 2MG/ML

Approval Date : 1987-12-23

Application Number : 50629

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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09

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DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 200MG/100ML

Approval Date : 1988-05-03

Application Number : 50629

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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10

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DOXORUBICIN HYDROCHLORIDE

Brand Name : DOXORUBICIN HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 150MG/75ML

Approval Date : 2011-03-28

Application Number : 50629

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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