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)
01 11CAPSULE, EXTENDED RELEASE;ORAL
02 4CAPSULE;ORAL
03 2INJECTABLE;INJECTION
04 1SOLUTION/DROPS;OTIC
05 1SOLUTION;IRRIGATION
06 1SOLUTION;ORAL
07 2SUSPENSION;ORAL
08 2SYRUP;ORAL
09 1TABLET, DELAYED RELEASE;ORAL
10 5TABLET, EXTENDED RELEASE;ORAL
11 3TABLET; ORAL
12 28TABLET;ORAL
01 10.025MG;2.5MG
02 11.5MG/AMP
03 4100MG
04 1100MG/5ML
05 110MG
06 112.5MG/5ML;10MG/5ML
07 1120MG
08 2125MG
09 1160MG
10 1167MG/5ML;167MG/5ML;167MG/5ML
11 1167MG;167MG;167MG
12 11GM
13 11MG
14 12.5MG
15 4200MG
16 120MG
17 1250MG
18 425MG
19 2300MG
20 1325MG;50MG
21 1325MG;50MG;40MG
22 1333MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 535MG
24 1400MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 1450MG
26 3500MG
27 2500MG;5MG
28 250MG
29 150MG/5ML
30 25MG
31 15MG/ML
32 15MG/ML;EQ 10,000 UNITS BASE/ML
33 160MG
34 1750MG
35 175MG
36 180MG
37 1EQ 10MG BASE
38 1EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
39 1EQ 20MG BASE
40 1EQ 5MG BASE
41 1N/A
01 58DISCN
02 3Blank
RLD : Yes
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : CAMPRAL
Dosage Strength : 333MG **Federal Register...
Approval Date : 2004-07-29
Application Number : 21431
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : BANCAP
Dosage Strength : 325MG;50MG
Approval Date : 1986-01-16
Application Number : 88889
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET; ORAL
Proprietary Name : ESGIC
Dosage Strength : 325MG;50MG;40MG
Approval Date : 1988-12-23
Application Number : 89660
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : DURADYNE DHC
Dosage Strength : 500MG;5MG
Approval Date : 1983-03-17
Application Number : 87809
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : CAPSULE; ORAL
Proprietary Name : BANCAP HC
Dosage Strength : 500MG;5MG
Approval Date : 1983-03-17
Application Number : 87961
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : DIPHENOXYLATE HYDROCHLOR...
Dosage Strength : 0.025MG;2.5MG
Approval Date : 1982-01-01
Application Number : 85509
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
BROMODIPHENHYDRAMINE HYDROCHLORIDE; CODEINE PHOSPHATE
Dosage Form : SYRUP; ORAL
Proprietary Name : AMBENYL
Dosage Strength : 12.5MG/5ML;10MG/5ML
Approval Date : 1984-01-10
Application Number : 9319
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CARBAMAZEPINE
Dosage Strength : 200MG
Approval Date : 1986-08-14
Application Number : 70231
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; ORAL
Proprietary Name : CELEXA
Dosage Strength : EQ 10MG BASE/5ML **Feder...
Approval Date : 1999-12-22
Application Number : 21046
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CORTISONE ACETATE
Dosage Strength : 25MG
Approval Date : 1982-01-01
Application Number : 80731
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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