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01 1DR REDDYS

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PharmaCompass

01

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Pharma, Lab & Chemical Expo
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code : AP

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : CHLORPROMAZINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 25MG/ML

Approval Date : 1982-01-01

Application Number : 80365

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

Dr Reddy Company Banner

02

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : THORAZINE

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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 9149

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : THORAZINE

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Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 9149

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : THORAZINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 9149

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : THORAZINE

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 : 9149

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : THORAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 9149

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

07

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : THORAZINE

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 9149

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : THORAZINE

Dosage Form : SYRUP;ORAL

Dosage Strength : 10MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 9149

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE

Brand Name : THORAZINE

Dosage Form : SUPPOSITORY;RECTAL

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 : 9149

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

CHLORPROMAZINE HYDROCHLORIDE

Brand Name : THORAZINE

Dosage Form : CONCENTRATE;ORAL

Dosage Strength : 30MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 9149

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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