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Approved Drug Products containing Dexamethasone Phosphate listed in the FDA Orange Book. Original Data : FDA Website

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01 3ASPEN GLOBAL INC

02 1DR REDDYS

03 1ABRAXIS PHARM

04 1ALCON

05 1ALCON PHARMS LTD

06 2AMNEAL

07 2BAUSCH AND LOMB

08 1BEL MAR

09 1CENT PHARMS

10 1DELL LABS

11 2EPIC PHARMA LLC

12 3EUGIA PHARMA

13 6FRESENIUS KABI USA

14 2GENEYORK PHARMS

15 2GLAND PHARMA LTD

16 3HIKMA

17 1INTL MEDICATION

18 1LUITPOLD

19 1LYPHOMED

20 8MERCK

21 1MICRO LABS

22 2MYLAN LABS LTD

23 3PHARMAFAIR

24 4QUAD PHARMS

25 1SANDOZ

26 2SOLA BARNES HIND

27 1SOMERSET

28 2SOMERSET THERAPS LLC

29 2TEVA PARENTERAL

30 2UCB INC

31 4WATSON LABS

32 1WYETH AYERST

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PharmaCompass

01

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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : HEXADROL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 14694

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Aspen API Comapny 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 :

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : DEXAMETHASONE SODIUM PHOSPHATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG PHOSPHATE/ML

Approval Date : 1986-04-09

Application Number : 89169

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Dr Reddy Company Banner

03

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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : HEXADROL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 14694

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Aspen API Comapny Banner

04

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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : HEXADROL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 20MG PHOSPHATE/ML

Approval Date : 1982-01-01

Application Number : 14694

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Aspen API Comapny Banner

05

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : DECADRON

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : EQ 0.05% PHOSPHATE

Approval Date : 1982-01-01

Application Number : 11977

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : DECADRON

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.1% PHOSPHATE

Approval Date : 1982-01-01

Application Number : 11983

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : DECADRON

Dosage Form : SOLUTION/DROPS;OPHTHALMIC, OTIC

Dosage Strength : EQ 0.1% PHOSPHATE

Approval Date : 1982-01-01

Application Number : 11984

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : DECADRON

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12071

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE

Brand Name : DECADRON

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12071

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DEXAMETHASONE SODIUM PHOSPHATE; LIDOCAINE HYDROCHLORIDE

Brand Name : DECADRON W/ XYLOCAINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4MG PHOSPHATE/ML;10MG/ML

Approval Date : 1982-01-01

Application Number : 13334

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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