Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
01 5STRIDES PHARMA
02 6ACTAVIS GROUP
03 3AIPING PHARM INC
04 6AUROBINDO PHARMA LTD
05 6CHARTWELL RX
06 6DURAMED PHARMS BARR
07 6INNOGENIX
08 6LEDERLE
09 6MANKIND PHARMA
10 6MSN
11 6MYLAN
12 6ORTHO MCNEIL
13 1ORTHO MCNEIL PHARM
14 1PAR PHARM
15 6PUREPAC PHARM
16 4QUANTUM PHARMICS
17 6ROYCE LABS
18 1SAGENT PHARMS
19 3SANDOZ
20 3SCIEGEN PHARMS INC
21 6SCS
22 6UPSHER SMITH LABS
23 4VINTAGE
24 12WATSON LABS
25 6ZYDUS PHARMS USA
01 1INJECTABLE; INJECTION
02 126TABLET;ORAL
01 69DISCN
02 50RX
03 8Blank
01 6HALDOL
02 1HALDOL SOLUTAB
03 120HALOPERIDOL
01 113No
02 6Yes
03 8Blank
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 2MG
Approval Date : 1986-11-03
Application Number : 71235
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.5MG
Approval Date : 1986-11-03
Application Number : 71235
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG
Approval Date : 1986-11-03
Application Number : 71235
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 1986-11-03
Application Number : 71235
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1987-07-20
Application Number : 71235
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : HALDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 15921
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : HALDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 15921
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : HALDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 15921
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : HALDOL
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 15921
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : HALDOL
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 : 15921
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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