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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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01 8CAPSULE, DELAYED REL PELLETS;ORAL
02 3CAPSULE, DELAYED RELEASE;ORAL
03 8CAPSULE;ORAL
04 9SYRUP;ORAL
05 52TABLET, DELAYED RELEASE;ORAL
06 2TABLET, EXTENDED RELEASE; ORAL
07 27TABLET, EXTENDED RELEASE;ORAL
08 2Tablet, Extended Release; Oral
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01 39DISCN
02 67RX
03 5Blank
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01 2DEPAKENE
02 4DEPAKOTE
03 2DEPAKOTE CP
04 6DEPAKOTE ER
05 79DIVALPROEX SODIUM
06 3STAVZOR
07 15VALPROIC ACID
01 95No
02 11Yes
03 5Blank
RLD : Yes
TE Code :
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Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
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
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD :
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code : AB
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
RLD : Yes
TE Code : AB
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
RLD : Yes
TE Code : AB
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
RLD : Yes
TE Code : AB
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
RLD : Yes
TE Code : AB
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
RLD : Yes
TE Code : AB
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