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 4METHYLNALTREXONE BROMIDE
11 2METOCLOPRAMIDE HYDROCHLORIDE
12 5OMEPRAZOLE; SODIUM BICARBONATE
13 1PLECANATIDE
14 3RIFAXIMIN
15 2SODIUM PHOSPHATE, DIBASIC, ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
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 3SOLUTION;SUBCUTANEOUS
09 1SUSPENSION;ORAL
10 2TABLET, CHEWABLE;ORAL
11 3TABLET, EXTENDED RELEASE;ORAL
12 2TABLET, ORALLY DISINTEGRATING;ORAL
13 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02 10.398GM;1.102GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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/PACKET;1.68GM/PACKET
10 120MG;1.1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 1250MG/5ML
12 12MG/ACTUATION
13 1343MG;20MG;750MG
14 1343MG;40MG;750MG
15 1375MG
16 13MG
17 14.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM
18 140MG
19 140MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 240MG/PACKET;1.68GM/PACKET
21 140MG;1.1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 1500MG
23 2550MG
24 17.54GM;140GM;2.2GM;48.11GM;5.2GM;9GM
25 1700MG;20MG;600MG
26 1700MG;40MG;600MG
27 18MG/0.4ML (8MG/0.4ML)
28 19MG
29 1EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 1EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 15DISCN
02 16RX
03 2Blank
RLD : Yes
TE Code : AA
ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE
Dosage Form : FOR SOLUTION; ORAL
Proprietary Name : MOVIPREP
Dosage Strength : 4.7GM;100GM;1.015GM;5.9G...
Approval Date : 2006-08-02
Application Number : 21881
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AA
RLD : Yes
TE Code :
ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE
Dosage Form : FOR SOLUTION; ORAL
Proprietary Name : PLENVU
Dosage Strength : 7.54GM;140GM;2.2GM;48.11...
Approval Date : 2018-05-04
Application Number : 209381
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : UCERIS
Dosage Strength : 9MG
Approval Date : 2013-01-14
Application Number : 203634
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : AEROSOL, FOAM; RECTAL
Proprietary Name : UCERIS
Dosage Strength : 2MG/ACTUATION
Approval Date : 2014-10-07
Application Number : 205613
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : DIURIL
Dosage Strength : 250MG/5ML
Approval Date : 1982-01-01
Application Number : 11870
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : PEPCID
Dosage Strength : 40MG/5ML **Federal Regis...
Approval Date : 1987-02-02
Application Number : 19527
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FENOGLIDE
Dosage Strength : 40MG
Approval Date : 2007-08-10
Application Number : 22118
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FENOGLIDE
Dosage Strength : 120MG
Approval Date : 2007-08-10
Application Number : 22118
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AT
Dosage Form : CREAM; TOPICAL
Proprietary Name : ANUSOL HC
Dosage Strength : 2.5%
Approval Date : 1984-06-06
Application Number : 88250
RX/OTC/DISCN : RX
RLD : No
TE Code : AT
RLD : No
TE Code :
MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE
Dosage Form : TABLET; ORAL
Proprietary Name : MAGNESIUM HYDROXIDE AND ...
Dosage Strength : 343MG;20MG;750MG
Approval Date : 2009-12-04
Application Number : 22456
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
