01 2ACETAMINOPHEN; CODEINE PHOSPHATE
02 5AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
03 1ASPIRIN; BUTALBITAL; CAFFEINE
04 2ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
05 1CARISOPRODOL
06 2CEFUROXIME AXETIL
07 2CHLORPROMAZINE HYDROCHLORIDE
08 1CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
09 3CITALOPRAM HYDROBROMIDE
10 1DICYCLOMINE HYDROCHLORIDE
11 4DIPHENHYDRAMINE HYDROCHLORIDE
12 3ESTRADIOL VALERATE
13 1FLUOXETINE HYDROCHLORIDE
14 4GUANFACINE HYDROCHLORIDE
15 1HALOPERIDOL LACTATE
16 2LEFLUNOMIDE
17 4LEVETIRACETAM
18 4METRONIDAZOLE
19 2MYCOPHENOLIC SODIUM
20 1NALTREXONE HYDROCHLORIDE
21 2NAPROXEN
22 3PEMOLINE
23 1PHENYLBUTAZONE
24 1PREDNISOLONE
25 1PROPRANOLOL HYDROCHLORIDE
26 2SULFAMETHOXAZOLE; TRIMETHOPRIM
27 3SUMATRIPTAN SUCCINATE
28 4SUNITINIB MALATE
29 2TRIAMCINOLONE DIACETATE
01 8CAPSULE;ORAL
02 2CONCENTRATE;ORAL
03 8INJECTABLE;INJECTION
04 4TABLET, DELAYED RELEASE;ORAL
05 5TABLET, EXTENDED RELEASE;ORAL
06 38TABLET;ORAL
01 20.025MG;2.5MG
02 1100MG
03 1100MG/ML
04 110MG
05 210MG/ML
06 110MG;2MG
07 110MG;4MG
08 118.75MG
09 11GM
10 11MG/ML
11 120MG
12 120MG/ML
13 1212.6MG;EQ 287.5MG BASE
14 3250MG
15 225MG
16 125MG/ML
17 125MG;2MG
18 125MG;4MG
19 1300MG;30MG
20 1300MG;60MG
21 130MG/ML
22 1325MG;50MG;40MG
23 1350MG
24 137.5MG
25 1375MG
26 1400MG;80MG
27 140MG/ML
28 140MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 4500MG
30 350MG
31 150MG;4MG
32 15MG
33 1750MG
34 175MG
35 1800MG;160MG
36 1EQ 100MG BASE
37 2EQ 10MG BASE
38 1EQ 12.5MG BASE
39 1EQ 180MG BASE
40 1EQ 1MG BASE
41 1EQ 20MG BASE
42 1EQ 250MG BASE
43 2EQ 25MG BASE
44 1EQ 2MG BASE
45 1EQ 360MG BASE
46 1EQ 37.5MG BASE
47 1EQ 3MG BASE
48 1EQ 40MG BASE
49 1EQ 4MG BASE
50 1EQ 500MG BASE
51 2EQ 50MG BASE
52 1EQ 5MG BASE/ML
01 51DISCN
02 14RX
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 300MG;60MG
Approval Date : 1992-07-16
Application Number : 81249
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 300MG;30MG
Approval Date : 1992-07-16
Application Number : 81250
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 10MG;2MG
Approval Date : 1987-11-27
Application Number : 71062
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 25MG;2MG
Approval Date : 1987-11-27
Application Number : 71063
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 25MG;4MG
Approval Date : 1987-11-27
Application Number : 71064
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 10MG;4MG
Approval Date : 1987-12-21
Application Number : 71862
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 50MG;4MG
Approval Date : 1987-12-21
Application Number : 71863
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL, ASPIRIN AND ...
Dosage Strength : 325MG;50MG;40MG
Approval Date : 1984-04-06
Application Number : 86398
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : LONOX
Dosage Strength : 0.025MG;2.5MG
Approval Date : 1982-01-01
Application Number : 85311
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 : 86173
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
