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 6CHARTWELL RX
12 5CYCLE
13 1DEVA HLDING
14 1EUGIA PHARMA
15 2FOSUN PHARMA
16 2GENUS
17 1GLAND
18 16GLAXOSMITHKLINE
19 5GLENMARK PHARMS LTD
20 3HIKMA
21 5IVAX SUB TEVA PHARMS
22 5KV PHARM
23 5LANNETT CO INC
24 5LEDERLE
25 5LUPIN
26 1MARSAM PHARMS LLC
27 4MSN
28 5PARKE DAVIS
29 2PHARM ASSOC
30 5PUREPAC PHARM
31 3PVT FORM
32 5SUN PHARM
33 5TEVA PHARMS
34 1THINQ PHARM-CRO PVT
35 5UPSHER SMITH LABS
36 3VANGARD
37 6WATSON LABS
38 5WEST WARD
39 2WOCKHARDT
40 1WYETH AYERST
41 5ZAMEER PHARMS
42 5ZYDUS LIFESCIENCES
43 1ZYDUS PHARMS
01 5CAPSULE, EXTENDED RELEASE;ORAL
02 13CONCENTRATE;ORAL
03 13INJECTABLE;INJECTION
04 2SUPPOSITORY;RECTAL
05 3SYRUP;ORAL
06 125TABLET;ORAL
01 87DISCN
02 74RX
01 135CHLORPROMAZINE HYDROCHLORIDE
02 2CHLORPROMAZINE HYDROCHLORIDE INTENSOL
03 5PROMAPAR
04 3SONAZINE
05 16THORAZINE
01 149No
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
