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Approved Drug Products containing Prestwick3_000351 listed in the FDA Orange Book. Original Data : FDA Website

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01 6SANOFI AVENTIS US

02 2ABBOTT

03 2AJANTA PHARMA LTD

04 2ALEMBIC

05 2ALKEM LABS LTD

06 2AMNEAL PHARMS CO

07 4ANI PHARMS

08 2APPCO

09 2ASCOT

10 2AUROBINDO PHARMA USA

11 2AZURITY

12 2BARR LABS INC

13 3BOEHRINGER INGELHEIM

14 2CASPER PHARMA LLC

15 2CHARTWELL RX

16 1COSETTE

17 2DAVA PHARMS INC

18 2INVENTIA

19 3IVAX PHARMS

20 2KV PHARM

21 2MANKIND PHARMA

22 1MONARCH PHARMS

23 5MUTUAL PHARM

24 2MYLAN

25 3NATCO PHARMA

26 2NOSTRUM LABS

27 2NOVARTIS

28 2NOVAST LABS

29 2NOVITIUM PHARMA

30 3PAR PHARM

31 2PHARMOBEDIENT

32 1PIONEER PHARMS

33 2PLIVA

34 2PUREPAC PHARM

35 3SANDOZ

36 4SUN PHARM INDUSTRIES

37 2SUNNY

38 2SUPERPHARM

39 4TWI PHARMS

40 2UMEDICA

41 4UNICHEM

42 2USL PHARMA

43 2VANGARD

44 2WARNER CHILCOTT

45 7WATSON LABS

46 4ZYDUS PHARMS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : Yes

TE Code :

CHLORTHALIDONE

Brand Name : HYGROTON

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12283

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Sanofi Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : Yes

TE Code :

CHLORTHALIDONE

Brand Name : HYGROTON

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12283

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Sanofi Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

CHLORTHALIDONE; RESERPINE

Brand Name : REGROTON

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG;0.25MG

Approval Date : 1982-01-01

Application Number : 15103

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

CHLORTHALIDONE; RESERPINE

Brand Name : DEMI-REGROTON

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;0.125MG

Approval Date : 1982-01-01

Application Number : 15103

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE

Brand Name : KERLEDEX

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;12.5MG

Approval Date : 1992-10-30

Application Number : 19807

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

RLD : No

TE Code :

BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE

Brand Name : KERLEDEX

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG;12.5MG

Approval Date : 1992-10-30

Application Number : 19807

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Sanofi Company Banner

07

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CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE

Brand Name : COMBIPRES

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG;0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 17503

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

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CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE

Brand Name : COMBIPRES

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG;0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 17503

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

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CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE

Brand Name : COMBIPRES

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1984-04-10

Application Number : 17503

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

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ATENOLOL; CHLORTHALIDONE

Brand Name : TENORETIC 100

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG;25MG

Approval Date : 1984-06-08

Application Number : 18760

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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