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01 1DR REDDYS

02 1MANKIND PHARMA

03 1ALEMBIC

04 3ASTRAZENECA

05 1ASTRAZENECA AB

06 1COVIS

07 1DEVA HOLDING AS

08 1LEXENPHARM

09 1LUPIN

10 1MICRO LABS

11 2MYLAN

12 3NOVARTIS

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17 1WILSHIRE PHARMS INC

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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 : AN

FORMOTEROL FUMARATE

Brand Name : FORMOTEROL FUMARATE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02MG/2ML

Approval Date : 2025-01-30

Application Number : 215907

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AN

FORMOTEROL FUMARATE

Brand Name : FORMOTEROL FUMARATE

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02MG/2ML

Approval Date : 2023-03-22

Application Number : 215883

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

Company Banner

03

BePharma
Not Confirmed
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BePharma
Not Confirmed

BUDESONIDE; FORMOTEROL FUMARATE DIHYDRATE

Brand Name : SYMBICORT

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.08MG/INH;0.0045MG/INH

Approval Date : 2006-07-21

Application Number : 21929

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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04

BePharma
Not Confirmed
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BePharma
Not Confirmed

BUDESONIDE; FORMOTEROL FUMARATE DIHYDRATE

Brand Name : SYMBICORT

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.16MG/INH;0.0045MG/INH

Approval Date : 2006-07-21

Application Number : 21929

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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05

BePharma
Not Confirmed
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BePharma
Not Confirmed

FORMOTEROL FUMARATE

Brand Name : FORADIL

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.012MG/INH **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2001-02-16

Application Number : 20831

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

BePharma
Not Confirmed
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BePharma
Not Confirmed

FORMOTEROL FUMARATE

Brand Name : FORADIL

Dosage Form : POWDER; INHALATION

Dosage Strength : 0.012MG/INH

Approval Date :

Application Number : 21279

RX/OTC/DISCN :

RLD :

TE Code :

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07

BePharma
Not Confirmed
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BePharma
Not Confirmed

FORMOTEROL FUMARATE

Brand Name : FORADIL CERTIHALER

Dosage Form : POWDER;INHALATION

Dosage Strength : 0.0085MG/INH

Approval Date : 2006-12-15

Application Number : 21592

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

BePharma
Not Confirmed
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BePharma
Not Confirmed

FORMOTEROL FUMARATE; MOMETASONE FUROATE

Brand Name : DULERA

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.005MG/INH;0.1MG/INH

Approval Date : 2010-06-22

Application Number : 22518

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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09

BePharma
Not Confirmed
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BePharma
Not Confirmed

FORMOTEROL FUMARATE; MOMETASONE FUROATE

Brand Name : DULERA

Dosage Form : AEROSOL, METERED;INHALATION

Dosage Strength : 0.005MG/INH;0.2MG/INH

Approval Date : 2010-06-22

Application Number : 22518

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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10

VIATRIS SPECIALTY

Country
BePharma
Not Confirmed
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VIATRIS SPECIALTY

Country
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BePharma
Not Confirmed

FORMOTEROL FUMARATE

Brand Name : PERFOROMIST

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 0.02MG/2ML

Approval Date : 2007-05-11

Application Number : 22007

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AN

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