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Approved Drug Products containing Tox21_300270 listed in the FDA Orange Book. Original Data : FDA Website

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01 4DR REDDYS LABS INC

02 4ACCORD HLTHCARE

03 4APNAR PHARMA LP

04 4APOTEX

05 4AUROBINDO PHARMA

06 4BIOCON PHARMA

07 10BRISTOL MYERS SQUIBB

08 4CHARTWELL RX

09 4CIPLA

10 4GLENMARK PHARMS LTD

11 3HISUN PHARM HANGZHOU

12 8NORVIUM BIOSCIENCE

13 5PLIVA HRVATSKA DOO

14 4RANBAXY LABS LTD

15 3TEVA

16 1TEVA PHARMS

17 4WATSON LABS

18 4ZYDUS PHARMS USA

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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

PRAVASTATIN SODIUM

Brand Name : PRAVASTATIN SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2006-10-23

Application Number : 76714

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

PRAVASTATIN SODIUM

Brand Name : PRAVASTATIN SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Approval Date : 2006-10-23

Application Number : 76714

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

03

  • 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

PRAVASTATIN SODIUM

Brand Name : PRAVASTATIN SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Approval Date : 2006-10-23

Application Number : 76714

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

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 : AB

PRAVASTATIN SODIUM

Brand Name : PRAVASTATIN SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 80MG

Approval Date : 2007-12-28

Application Number : 76714

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

05

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PRAVASTATIN SODIUM

Brand Name : PRAVACHOL

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1991-10-31

Application Number : 19898

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

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PRAVASTATIN SODIUM

Brand Name : PRAVACHOL

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1991-10-31

Application Number : 19898

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

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PRAVASTATIN SODIUM

Brand Name : PRAVACHOL

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1993-03-22

Application Number : 19898

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

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PRAVASTATIN SODIUM

Brand Name : PRAVACHOL

Dosage Form : TABLET;ORAL

Dosage Strength : 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2001-12-18

Application Number : 19898

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

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ASPIRIN; PRAVASTATIN SODIUM

Brand Name : PRAVIGARD PAC (COPACKAGED)

Dosage Form : TABLET;ORAL

Dosage Strength : 81MG;20MG

Approval Date : 2003-06-24

Application Number : 21387

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

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ASPIRIN; PRAVASTATIN SODIUM

Brand Name : PRAVIGARD PAC (COPACKAGED)

Dosage Form : TABLET;ORAL

Dosage Strength : 81MG;40MG

Approval Date : 2003-06-24

Application Number : 21387

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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