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01 8ABBVIE

02 2ABBVIE INC

03 1REDDYS

04 4ABBOTT

05 1ACTAVIS LABS FL INC

06 1AJANTA PHARMA LTD

07 2AMNEAL PHARMS

08 1ANI PHARMS

09 2ANNORA PHARMA

10 3APOTEX

11 5AUROBINDO PHARMA LTD

12 4BIONPHARMA

13 1CATALENT

14 4CHARTWELL RX

15 1COSETTE

16 5DR REDDYS LABS LTD

17 3ENDO OPERATIONS

18 1HIBROW HLTHCARE

19 1HIKMA

20 2IMPAX LABS

21 3INVATECH

22 1LANNETT CO INC

23 3LUPIN

24 2LUPIN LTD

25 5MYLAN

26 3NORVIUM BIOSCIENCE

27 1NOSTRUM LABS INC

28 3ORBION PHARMS

29 1PAR PHARM

30 1PHARM ASSOC

31 1PHARMOBEDIENT CNSLTG

32 3PRINSTON INC

33 1QUAGEN

34 1RISING

35 1SCHERER RP

36 3SUN PHARM INDS

37 1SUN PHARM INDS LTD

38 3TEVA

39 1TEVA PHARMS USA

40 2UNICHEM

41 3UNICHEM LABS LTD

42 4UPSHER SMITH LABS

43 2UTOPIC PHARMS

44 2WOCKHARDT

45 6ZYDUS PHARMS USA INC

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PharmaCompass

01

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Pharmtech & Ingredients
Not Confirmed

VALPROIC ACID

Brand Name : DEPAKENE

Dosage Form : CAPSULE;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Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 18081

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

RLD : No

TE Code : AB

DIVALPROEX SODIUM

Brand Name : DIVALPROEX SODIUM

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 500MG VALPROIC ACID

Approval Date : 2012-03-12

Application Number : 90070

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Dr Reddy Company Banner

03

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Pharmtech & Ingredients
Not Confirmed

VALPROIC ACID

Brand Name : DEPAKENE

Dosage Form : SYRUP;ORAL

Dosage Strength : 250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 18082

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Abbvie Company Banner

04

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Pharmtech & Ingredients
Not Confirmed

DIVALPROEX SODIUM

Brand Name : DEPAKOTE

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 250MG VALPROIC ACID

Approval Date : 1983-03-10

Application Number : 18723

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Abbvie Company Banner

05

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Pharmtech & Ingredients
Not Confirmed

DIVALPROEX SODIUM

Brand Name : DEPAKOTE

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 500MG VALPROIC ACID

Approval Date : 1983-03-10

Application Number : 18723

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Abbvie Company Banner

06

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Pharmtech & Ingredients
Not Confirmed

DIVALPROEX SODIUM

Brand Name : DEPAKOTE

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 125MG VALPROIC ACID

Approval Date : 1984-10-26

Application Number : 18723

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Abbvie Company Banner

07

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Pharmtech & Ingredients
Not Confirmed

DIVALPROEX SODIUM

Brand Name : DEPAKOTE

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 125MG VALPROIC ACID

Approval Date : 1989-09-12

Application Number : 19680

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Abbvie Company Banner

08

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Pharmtech & Ingredients
Not Confirmed

DIVALPROEX SODIUM

Brand Name : DEPAKOTE ER

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 500MG VALPROIC ACID

Approval Date : 2000-08-04

Application Number : 21168

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Abbvie Company Banner

09

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Pharmtech & Ingredients
Not Confirmed

DIVALPROEX SODIUM

Brand Name : DEPAKOTE ER

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 250MG VALPROIC ACID

Approval Date : 2002-05-31

Application Number : 21168

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Abbvie Company Banner

10

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Pharmtech & Ingredients
Not Confirmed

DIVALPROEX SODIUM

Brand Name : DEPAKOTE ER

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Dosage Strength : 250MG

Approval Date :

Application Number : 22267

RX/OTC/DISCN :

RLD :

TE Code :

Abbvie Company Banner