01 1ABRAXIS PHARM
02 1ACTAVIS MID ATLANTIC
03 1ALPHARMA
04 2BAXTER HLTHCARE CORP
05 1EPIC PHARMA LLC
06 1FOSUN PHARMA
07 2FRESENIUS KABI USA
08 1GLAND PHARMA LTD
09 2HIKMA
10 1JANSSEN PHARMS
11 1LANNETT CO INC
12 2MARSAM PHARMS LLC
13 1MORTON GROVE
14 1MYLAN LABS LTD
15 1ORTHO MCNEIL
16 1PHARM ASSOC
17 1QUAD PHARMS
18 1RUBICON
19 2SAGENT PHARMS
20 1SCS
21 1SMITH AND NEPHEW
22 3SOLOPAK
23 1TEVA
24 1TEVA PHARMS
25 1TEVA PHARMS USA
26 3WATSON LABS
01 10CONCENTRATE;ORAL
02 23INJECTABLE;INJECTION
03 1Injectable; Injection
04 1SOLUTION;ORAL
01 24DISCN
02 10RX
03 1Blank
01 2HALDOL
02 31HALOPERIDOL
03 1HALOPERIDOL INTENSOL
04 1HALOPERIDOL LACTATE
01 32No
02 2Yes
03 1Blank
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML
Approval Date : 1988-05-17
Application Number : 70713
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML
Approval Date : 1988-05-17
Application Number : 70714
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML
Approval Date : 1988-05-17
Application Number : 70744
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : EQ 2MG BASE/ML
Approval Date : 1986-04-11
Application Number : 70318
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : HALDOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 15923
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : HALDOL
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 15922
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : EQ 2MG BASE/ML
Approval Date : 1986-03-07
Application Number : 70710
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML
Approval Date : 1987-12-14
Application Number : 70800
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML
Approval Date : 1987-12-14
Application Number : 70801
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HALOPERIDOL
Dosage Form : CONCENTRATE;ORAL
Dosage Strength : EQ 2MG BASE/ML
Approval Date : 1986-06-10
Application Number : 70726
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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