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Approved Drug Products containing MolPort-001-759-947 listed in the FDA Orange Book. Original Data : FDA Website

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01 3DR REDDYS LABS SA

02 3MIKART

03 1STRIDES PHARMA

04 1ACME LABS

05 2ACTAVIS ELIZABETH

06 3AUROBINDO PHARMA LTD

07 1BARR

08 1BELCHER

09 4COREPHARMA

10 2ENDO OPERATIONS

11 1FERNDALE LABS

12 2GLENMARK PHARMS LTD

13 2I3 PHARMS

14 1JANSSEN R AND D

15 3NOVITIUM PHARMA

16 2OHM LABS

17 1ORTHO MCNEIL PHARM

18 2PIONEER PHARMS

19 5RISING PHARMA

20 2SENORES PHARMS

21 1SUN PHARM INDUSTRIES

22 2TEVA PHARMS USA INC

23 2UPSHER SMITH LABS

24 6WATSON LABS

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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

CHLORZOXAZONE

Brand Name : CHLORZOXAZONE

Dosage Form : TABLET;ORAL

Dosage Strength : 375MG

Approval Date : 2020-07-21

Application Number : 211849

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAs a CDMO, Mikart offers integrated CDMO services for Solid Dose & Non-sterile Liquid formulations.

RLD : No

TE Code : AB

CHLORZOXAZONE

Brand Name : CHLORZOXAZONE

Dosage Form : TABLET;ORAL

Dosage Strength : 375MG

Approval Date : 2010-06-01

Application Number : 40861

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Mikart

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code :

CHLORZOXAZONE

Brand Name : CHLORZOXAZONE

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG

Approval Date : 1983-09-20

Application Number : 87981

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

04

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code : AA

CHLORZOXAZONE

Brand Name : CHLORZOXAZONE

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG

Approval Date : 2020-07-21

Application Number : 211849

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

Dr Reddy Company Banner

05

  • 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

CHLORZOXAZONE

Brand Name : CHLORZOXAZONE

Dosage Form : TABLET;ORAL

Dosage Strength : 750MG

Approval Date : 2020-07-21

Application Number : 211849

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAs a CDMO, Mikart offers integrated CDMO services for Solid Dose & Non-sterile Liquid formulations.

RLD : No

TE Code : AB

CHLORZOXAZONE

Brand Name : CHLORZOXAZONE

Dosage Form : TABLET;ORAL

Dosage Strength : 750MG

Approval Date : 2010-06-01

Application Number : 40861

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Mikart

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAs a CDMO, Mikart offers integrated CDMO services for Solid Dose & Non-sterile Liquid formulations.

RLD : No

TE Code : AA

CHLORZOXAZONE

Brand Name : CHLORZOXAZONE

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG

Approval Date : 2016-06-24

Application Number : 207483

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

Mikart

08

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

CHLORZOXAZONE

Brand Name : CHLORZOXAZONE

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG

Approval Date : 1995-09-29

Application Number : 40113

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

CHLORZOXAZONE

Brand Name : PARAFON FORTE DSC

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1987-06-15

Application Number : 11529

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

CHLORZOXAZONE

Brand Name : PARAFLEX

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 11300

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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