01 8ABBVIE
02 2ABBVIE INC
03 1REDDYS
04 1MANKIND PHARMA
05 4ABBOTT
06 1ACTAVIS LABS FL INC
07 1ADARE PHARMS INC
08 1AJANTA PHARMA LTD
09 1ALEMBIC
10 2AMNEAL PHARMS
11 1ANI PHARMS
12 2ANNORA PHARMA
13 3APOTEX
14 4AUROBINDO PHARMA LTD
15 3BIONPHARMA
16 1CATALENT
17 1CHARTWELL
18 5CHARTWELL RX
19 1COSETTE
20 4DR REDDYS LABS LTD
21 2HETERO LABS LTD III
22 1HIBROW HLTHCARE
23 1HIKMA
24 1HQ SPCLT PHARMA
25 2IMPAX LABS
26 3INVATECH
27 1LANNETT CO INC
28 5LUPIN
29 5MYLAN
30 3ORBION PHARMS
31 1PAI HOLDINGS
32 1PAR PHARM
33 1PH HEALTH
34 1PHARM ASSOC
35 5PHARMOBEDIENT
36 1PHARMOBEDIENT CNSLTG
37 3PRINSTON INC
38 1QUAGEN
39 1RISING
40 1SCHERER RP
41 2SCIEGEN PHARMS
42 3SUN PHARM INDS
43 1SUN PHARM INDS LTD
44 3TEVA
45 1TEVA PHARMS
46 1TEVA PHARMS USA
47 2UNICHEM
48 3UNICHEM LABS LTD
49 3UPSHER SMITH LABS
50 1WATSON LABS
51 2YICHANG HUMANWELL
52 6ZYDUS PHARMS USA INC
01 8CAPSULE, DELAYED REL PELLETS;ORAL
02 3CAPSULE, DELAYED RELEASE;ORAL
03 1CAPSULE, EXTENDED RELEASE;ORAL
04 7CAPSULE;ORAL
05 1POWDER;INTRAVENOUS
06 1SOLUTION/DROPS;OPHTHALMIC
07 9SYRUP;ORAL
08 51TABLET, DELAYED RELEASE;ORAL
09 2TABLET, EXTENDED RELEASE; ORAL
10 24TABLET, EXTENDED RELEASE;ORAL
11 6TABLET;ORAL
12 2Tablet, Extended Release; Oral
01 41DISCN
02 70RX
03 4Blank
01 2DEPAKENE
02 4DEPAKOTE
03 2DEPAKOTE CP
04 6DEPAKOTE ER
05 75DIVALPROEX SODIUM
06 1DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE
07 2FINASTERIDE
08 1IMIPENEM AND CILASTATIN
09 2LAMOTRIGINE
10 1PROPRANOLOL HYDROCHLORIDE
11 1QUASENSE
12 3STAVZOR
13 1TOPIRAMATE
14 14VALPROIC ACID
01 100No
02 11Yes
03 4Blank
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Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : No
TE Code : AB
Brand Name : DIVALPROEX SODIUM
Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL
Dosage Strength : EQ 125MG VALPROIC ACID
Approval Date : 2025-08-12
Application Number : 217358
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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
