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01 4ABLE

02 4ACTAVIS ELIZABETH

03 4AMNEAL PHARM

04 2ASCOT

05 7CHARTWELL RX

06 3GLENWOOD

07 4HERITAGE PHARMA

08 4IMPAX LABS

09 1IVAX SUB TEVA PHARMS

10 3LANNETT

11 4LANNETT CO INC

12 9ODYSSEY PHARMS

13 1QUAD PHARMS

14 5SANDOZ

15 4SUN PHARM INDS INC

16 4UPSHER SMITH LABS

17 11WATSON LABS

18 4WOCKHARDT

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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : URECHOLINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 6536

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : URECHOLINE

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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 6536

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : URECHOLINE

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Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 6536

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : URECHOLINE

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Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 6536

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : URECHOLINE

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 : 6536

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : BETHANECHOL CHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2004-07-27

Application Number : 40483

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : BETHANECHOL CHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG

Approval Date : 2004-07-27

Application Number : 40485

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : BETHANECHOL CHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Approval Date : 2004-07-27

Application Number : 40492

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : BETHANECHOL CHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Approval Date : 2004-07-27

Application Number : 40509

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BETHANECHOL CHLORIDE

Brand Name : BETHANECHOL CHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Approval Date : 2003-09-29

Application Number : 40518

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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