01 2ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE
02 2BUDESONIDE
03 1CHLOROTHIAZIDE
04 1FAMOTIDINE
05 2FENOFIBRATE
06 1HYDROCORTISONE
07 4MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE
08 1MESALAMINE
09 2METFORMIN HYDROCHLORIDE
10 5METHYLNALTREXONE BROMIDE
11 2METOCLOPRAMIDE HYDROCHLORIDE
12 5OMEPRAZOLE; SODIUM BICARBONATE
13 1PLECANATIDE
14 4RIFAXIMIN
15 2SODIUM PHOSPHATE, DIBASIC, ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
01 12SALIX
02 2SALIX PHARMACEUTICALS INC
03 14SALIX PHARMS
04 5SANTARUS
05 2SANTARUS INC
01 1AEROSOL, FOAM;RECTAL
02 1CAPSULE, EXTENDED RELEASE;ORAL
03 2CAPSULE;ORAL
04 1CREAM;TOPICAL
05 2FOR SOLUTION;ORAL
06 1FOR SUSPENSION; ORAL
07 3FOR SUSPENSION;ORAL
08 1SOLUTION
09 3SOLUTION;SUBCUTANEOUS
10 1SUSPENSION;ORAL
11 1TABLET
12 2TABLET, CHEWABLE;ORAL
13 3TABLET, EXTENDED RELEASE;ORAL
14 2TABLET, ORALLY DISINTEGRATING;ORAL
15 11TABLET;ORAL
01 10.398GM;1.102GM
02 10.398GM;1.102GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 1120MG
04 212MG/0.6ML (12MG/0.6ML)
05 1150MG
06 11GM
07 12.5%
08 1200MG
09 120MG/ML
10 120MG/PACKET;1.68GM/PACKET
11 120MG;1.1GM
12 1250MG/5ML
13 12MG/ACTUATION
14 1343MG;20MG;750MG
15 1343MG;40MG;750MG
16 1375MG
17 13MG
18 14.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM
19 140MG
20 140MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 240MG/PACKET;1.68GM/PACKET
22 140MG;1.1GM
23 1500MG
24 3550MG
25 17.54GM;140GM;2.2GM;48.11GM;5.2GM;9GM
26 1700MG;20MG;600MG
27 1700MG;40MG;600MG
28 18MG/0.4ML (8MG/0.4ML)
29 19MG
30 1EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 1EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 2Canada
02 33USA
Regulatory Info : RX
Registration Country : USA
ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE
Dosage Form : FOR SOLUTION;ORAL
Brand Name : MOVIPREP
Dosage Strength : 4.7GM;100GM;1.015GM;5....
Packaging :
Approval Date : 2006-08-02
Application Number : 21881
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE
Dosage Form : FOR SOLUTION;ORAL
Brand Name : PLENVU
Dosage Strength : 7.54GM;140GM;2.2GM;48....
Packaging :
Approval Date : 2018-05-04
Application Number : 209381
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : UCERIS
Dosage Strength : 9MG
Packaging :
Approval Date : 2013-01-14
Application Number : 203634
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : AEROSOL, FOAM;RECTAL
Brand Name : UCERIS
Dosage Strength : 2MG/ACTUATION
Packaging :
Approval Date : 2014-10-07
Application Number : 205613
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SUSPENSION;ORAL
Brand Name : DIURIL
Dosage Strength : 250MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 11870
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : PEPCID
Dosage Strength : 40MG/5ML **Federal Reg...
Packaging :
Approval Date : 1987-02-02
Application Number : 19527
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FENOGLIDE
Dosage Strength : 40MG
Packaging :
Approval Date : 2007-08-10
Application Number : 22118
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : FENOGLIDE
Dosage Strength : 120MG
Packaging :
Approval Date : 2007-08-10
Application Number : 22118
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : ANUSOL HC
Dosage Strength : 2.5%
Packaging :
Approval Date : 1984-06-06
Application Number : 88250
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE
Dosage Form : TABLET;ORAL
Brand Name : MAGNESIUM HYDROXIDE AND O...
Dosage Strength : 343MG;20MG;750MG
Packaging :
Approval Date : 2009-12-04
Application Number : 22456
Regulatory Info : DISCN
Registration Country : USA
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