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 1ASPIRO
09 5AUROBINDO PHARMA LTD
10 11CHARTWELL RX
11 5CYCLE
12 1DEVA HLDING
13 1EUGIA PHARMA
14 2GENUS
15 1GLAND
16 16GLAXOSMITHKLINE
17 5GLENMARK PHARMS LTD
18 3HIKMA
19 5IVAX SUB TEVA PHARMS
20 5KV PHARM
21 5LANNETT CO INC
22 5LEDERLE
23 5LUPIN
24 1MARSAM PHARMS LLC
25 4MSN
26 5PARKE DAVIS
27 2PHARM ASSOC
28 5PUREPAC PHARM
29 3PVT FORM
30 2RUBICON
31 2SAPTALIS PHARMS
32 5SOMERSET THERAPS LLC
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 71RX
01 137CHLORPROMAZINE HYDROCHLORIDE
02 2CHLORPROMAZINE HYDROCHLORIDE INTENSOL
03 5PROMAPAR
04 3SONAZINE
05 16THORAZINE
01 151No
02 12Yes
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
