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Approved Drug Products containing NCGC00024667-10 listed in the FDA Orange Book. Original Data : FDA Website

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01 7STRIDES PHARMA

02 3ACCORD HLTHCARE

03 7CHARTWELL RX

04 4DAVA PHARMS INC

05 2DURAMED PHARMS BARR

06 3HALSEY

07 2HERITAGE PHARMA

08 4IVAX SUB TEVA PHARMS

09 10MERCK

10 1MYLAN

11 2PAR PHARM

12 7PARKE DAVIS

13 3PLIVA

14 7PUREPAC PHARM

15 2RISING

16 2RISING PHARMA

17 3ROXANE

18 2SANDOZ

19 3SUN PHARM INDUSTRIES

20 2SUPERPHARM

21 7TEVA

22 20WATSON LABS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code :

METHYLDOPA

Brand Name : METHYLDOPA

Dosage Form : TABLET;ORAL

Dosage Strength : 125MG

Approval Date : 1987-01-02

Application Number : 70535

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

02

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code :

METHYLDOPA

Brand Name : METHYLDOPA

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG

Approval Date : 1987-01-02

Application Number : 70536

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code :

METHYLDOPA

Brand Name : METHYLDOPA

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG

Approval Date : 1987-01-02

Application Number : 70537

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

04

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code :

HYDROCHLOROTHIAZIDE; METHYLDOPA

Brand Name : METHYLDOPA AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;250MG

Approval Date : 1987-02-02

Application Number : 70612

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

05

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code :

HYDROCHLOROTHIAZIDE; METHYLDOPA

Brand Name : METHYLDOPA AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG;500MG

Approval Date : 1987-02-02

Application Number : 70613

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

06

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code :

HYDROCHLOROTHIAZIDE; METHYLDOPA

Brand Name : METHYLDOPA AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG;500MG

Approval Date : 1987-02-02

Application Number : 70614

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

07

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code :

HYDROCHLOROTHIAZIDE; METHYLDOPA

Brand Name : METHYLDOPA AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG;250MG

Approval Date : 1987-02-02

Application Number : 70616

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

08

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METHYLDOPA

Brand Name : ALDOMET

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 : 13400

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

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Not Confirmed
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Not Confirmed

METHYLDOPA

Brand Name : ALDOMET

Dosage Form : TABLET;ORAL

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

Approval Date : 1982-01-01

Application Number : 13400

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

Formnext Forum
Not Confirmed
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Formnext Forum
Not Confirmed

METHYLDOPA

Brand Name : ALDOMET

Dosage Form : TABLET;ORAL

Dosage Strength : 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 13400

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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