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01 5STRIDES PHARMA

02 6ACTAVIS GROUP

03 3AIPING PHARM INC

04 6AUROBINDO PHARMA LTD

05 6CHARTWELL RX

06 6DURAMED PHARMS BARR

07 6INNOGENIX

08 6LEDERLE

09 6MANKIND PHARMA

10 6MSN

11 6MYLAN

12 6ORTHO MCNEIL

13 1ORTHO MCNEIL PHARM

14 1PAR PHARM

15 6PUREPAC PHARM

16 4QUANTUM PHARMICS

17 6ROYCE LABS

18 1SAGENT PHARMS

19 3SANDOZ

20 3SCIEGEN PHARMS INC

21 6SCS

22 6UPSHER SMITH LABS

23 4VINTAGE

24 12WATSON LABS

25 6ZYDUS PHARMS USA

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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 :

HALOPERIDOL

Brand Name : HALOPERIDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG

Approval Date : 1986-11-03

Application Number : 71235

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 :

HALOPERIDOL

Brand Name : HALOPERIDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 0.5MG

Approval Date : 1986-11-03

Application Number : 71235

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 :

HALOPERIDOL

Brand Name : HALOPERIDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG

Approval Date : 1986-11-03

Application Number : 71235

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 :

HALOPERIDOL

Brand Name : HALOPERIDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Approval Date : 1986-11-03

Application Number : 71235

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 :

HALOPERIDOL

Brand Name : HALOPERIDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 1987-07-20

Application Number : 71235

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Strides Pharma Science

06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

HALOPERIDOL

Brand Name : HALDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 15921

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

07

Pharmtech & Ingredients
Not Confirmed
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arrow
Pharmtech & Ingredients
Not Confirmed

HALOPERIDOL

Brand Name : HALDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 15921

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

08

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HALOPERIDOL

Brand Name : HALDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 15921

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

09

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HALOPERIDOL

Brand Name : HALDOL

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 15921

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

HALOPERIDOL

Brand Name : HALDOL

Dosage Form : TABLET;ORAL

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

Approval Date : 1982-01-01

Application Number : 15921

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank