DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR REDDYS
02 5ABBOTT
03 1ABRAXIS PHARM
04 1ACTAVIS MID ATLANTIC
05 5ALEMBIC
06 1ALPHARMA US PHARMS
07 5AMNEAL PHARMS CO
08 5APPCO
09 1ASPIRO
10 5AUROBINDO PHARMA LTD
11 11CHARTWELL RX
12 5CYCLE
13 1DEVA HLDING
14 1EUGIA PHARMA
15 2GENUS
16 1GLAND
17 16GLAXOSMITHKLINE
18 5GLENMARK PHARMS LTD
19 3HIKMA
20 5IVAX SUB TEVA PHARMS
21 5KV PHARM
22 5LANNETT CO INC
23 5LEDERLE
24 5LUPIN
25 1MARSAM PHARMS LLC
26 4MSN
27 5PARKE DAVIS
28 2PHARM ASSOC
29 5PUREPAC PHARM
30 3PVT FORM
31 2RUBICON
32 2SAPTALIS PHARMS
33 5SUN PHARM
34 5TEVA PHARMS
35 1THINQ PHARM-CRO PVT
36 5UPSHER SMITH LABS
37 3VANGARD
38 6WATSON LABS
39 5WEST WARD
40 2WOCKHARDT
41 1WYETH AYERST
42 5ZYDUS LIFESCIENCES
43 1ZYDUS PHARMS
01 5CAPSULE, EXTENDED RELEASE;ORAL
02 15CONCENTRATE;ORAL
03 13INJECTABLE;INJECTION
04 2SUPPOSITORY;RECTAL
05 3SYRUP;ORAL
06 125TABLET;ORAL
01 92DISCN
02 69RX
03 2Blank
01 137CHLORPROMAZINE HYDROCHLORIDE
02 2CHLORPROMAZINE HYDROCHLORIDE INTENSOL
03 5PROMAPAR
04 3SONAZINE
05 16THORAZINE
01 149No
02 12Yes
03 2Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AP
Brand Name : CHLORPROMAZINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML
Approval Date : 1982-01-01
Application Number : 80365
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code :
Brand Name : THORAZINE
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 9149
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : THORAZINE
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Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 9149
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : THORAZINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 9149
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : THORAZINE
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 : 9149
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : THORAZINE
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 9149
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : THORAZINE
Dosage Form : TABLET;ORAL
Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 9149
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : THORAZINE
Dosage Form : SYRUP;ORAL
Dosage Strength : 10MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 9149
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : THORAZINE
Dosage Form : SUPPOSITORY;RECTAL
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 : 9149
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : THORAZINE
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : 30MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 9149
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
