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01 8ABBVIE

02 2ABBVIE INC

03 1REDDYS

04 1MANKIND PHARMA

05 4ABBOTT

06 1ACTAVIS LABS FL INC

07 1AJANTA PHARMA LTD

08 1ALEMBIC

09 2AMNEAL PHARMS

10 1ANI PHARMS

11 2ANNORA PHARMA

12 3APOTEX

13 5AUROBINDO PHARMA LTD

14 4BIONPHARMA

15 1CATALENT

16 4CHARTWELL RX

17 1COSETTE

18 5DR REDDYS LABS LTD

19 1HIBROW HLTHCARE

20 1HIKMA

21 2IMPAX LABS

22 3INVATECH

23 1LANNETT CO INC

24 3LUPIN

25 2LUPIN LTD

26 5MYLAN

27 3ORBION PHARMS

28 1PAI HOLDINGS

29 1PAR PHARM

30 3PH HEALTH

31 1PHARM ASSOC

32 3PHARMOBEDIENT

33 1PHARMOBEDIENT CNSLTG

34 3PRINSTON INC

35 1QUAGEN

36 1RISING

37 1SCHERER RP

38 2SCIEGEN PHARMS INC

39 3SUN PHARM INDS

40 1SUN PHARM INDS LTD

41 3TEVA

42 1TEVA PHARMS USA

43 2UNICHEM

44 3UNICHEM LABS LTD

45 4UPSHER SMITH LABS

46 2YICHANG HUMANWELL

47 6ZYDUS PHARMS USA INC

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PharmaCompass

01

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Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD :

TE Code :

DIVALPROEX SODIUM

Brand Name : DIVALPROEX SODIUM

Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL

Dosage Strength : EQ 125MG VALPROIC ACID

Approval Date :

Application Number : 217358

RX/OTC/DISCN :

RLD :

TE Code :

Company Banner

04

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Dosage Strength : 250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

05

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

06

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

07

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

08

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

09

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

10

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