01 1ACAMPROSATE CALCIUM
02 1ACETAMINOPHEN; BUTALBITAL
03 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE
04 2ACETAMINOPHEN; HYDROCODONE BITARTRATE
05 1ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
06 1BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE
07 1CARBAMAZEPINE
08 1CITALOPRAM HYDROBROMIDE
09 1CORTISONE ACETATE
10 2EPINEPHRINE
11 3ESCITALOPRAM OXALATE
12 3HYDROCHLOROTHIAZIDE
13 1HYDROCORTISONE
14 1HYDROCORTISONE; POLYMYXIN B SULFATE
15 1IBUPROFEN; OXYCODONE HYDROCHLORIDE
16 1INDOMETHACIN
17 2METHOCARBAMOL
18 2METHYLTESTOSTERONE
19 5PHENDIMETRAZINE TARTRATE
20 1PREDNISOLONE
21 3PREDNISONE
22 1PROCAINAMIDE HYDROCHLORIDE
23 1PROPIOLACTONE
24 4PROPRANOLOL HYDROCHLORIDE
25 2RAUWOLFIA SERPENTINA ROOT
26 1RIMANTADINE HYDROCHLORIDE
27 2SULFAMETHIZOLE
28 13THEOPHYLLINE
29 2TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE)
30 3colistimethate
01 21FOREST LABS
02 11FOREST PHARMS
03 1Forest Laboratories UK Limited,
04 2Forest Pharma BV
05 29INWOOD LABS
01 11CAPSULE, EXTENDED RELEASE;ORAL
02 4CAPSULE;ORAL
03 1INHALATION POWDER, HARD CAPSULE
04 2INJECTABLE;INJECTION
05 2POWDER FOR NEBULISER SOLUTION
06 1SOLUTION/DROPS;OTIC
07 1SOLUTION;IRRIGATION
08 1SOLUTION;ORAL
09 2SUSPENSION;ORAL
10 2SYRUP;ORAL
11 1TABLET, DELAYED RELEASE;ORAL
12 5TABLET, EXTENDED RELEASE;ORAL
13 3TABLET; ORAL
14 28TABLET;ORAL
01 10.025MG;2.5MG
02 11 MILLION IU
03 11.5MG/AMP
04 4100MG
05 1100MG/5ML
06 110MG
07 112.5MG/5ML;10MG/5ML
08 1120MG
09 2125MG
10 1160MG
11 11662500 IU
12 1167MG/5ML;167MG/5ML;167MG/5ML
13 1167MG;167MG;167MG
14 11GM
15 11MG
16 12 MILLION IU
17 12.5MG
18 4200MG
19 120MG
20 1250MG
21 425MG
22 2300MG
23 1325MG;50MG
24 1325MG;50MG;40MG
25 1333MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 535MG
27 1400MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 1450MG
29 3500MG
30 2500MG;5MG
31 250MG
32 150MG/5ML
33 25MG
34 15MG/ML
35 15MG/ML;EQ 10,000 UNITS BASE/ML
36 160MG
37 1750MG
38 175MG
39 180MG
40 1EQ 10MG BASE
41 1EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
42 1EQ 20MG BASE
43 1EQ 5MG BASE
44 1N/A
01 3Sweden
02 61USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, DELAYED RELEASE;...
Brand Name : CAMPRAL
Dosage Strength : 333MG **Federal Regist...
Packaging :
Approval Date : 2004-07-29
Application Number : 21431
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : BANCAP
Dosage Strength : 325MG;50MG
Packaging :
Approval Date : 1986-01-16
Application Number : 88889
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET;ORAL
Brand Name : ESGIC
Dosage Strength : 325MG;50MG;40MG
Packaging :
Approval Date : 1988-12-23
Application Number : 89660
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : DURADYNE DHC
Dosage Strength : 500MG;5MG
Packaging :
Approval Date : 1983-03-17
Application Number : 87809
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : CAPSULE;ORAL
Brand Name : BANCAP HC
Dosage Strength : 500MG;5MG
Packaging :
Approval Date : 1983-03-17
Application Number : 87961
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : DIPHENOXYLATE HYDROCHLORI...
Dosage Strength : 0.025MG;2.5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 85509
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE
Dosage Form : SYRUP;ORAL
Brand Name : AMBENYL
Dosage Strength : 12.5MG/5ML;10MG/5ML
Packaging :
Approval Date : 1984-01-10
Application Number : 9319
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CARBAMAZEPINE
Dosage Strength : 200MG
Packaging :
Approval Date : 1986-08-14
Application Number : 70231
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;ORAL
Brand Name : CELEXA
Dosage Strength : EQ 10MG BASE/5ML **Fed...
Packaging :
Approval Date : 1999-12-22
Application Number : 21046
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Dosage Form : POWDER FOR NEBULISER SOL...
Brand Name : Colineb
Dosage Strength : 1 MILLION IU
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Forest Laboratories is a supplier offers 15 products (APIs, Excipients or Intermediates).
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