01 3ACETAMINOPHEN; CODEINE PHOSPHATE
02 1ACETIC ACID, GLACIAL
03 1ACETIC ACID, GLACIAL; HYDROCORTISONE
04 2ALBUTEROL SULFATE
05 6AMITRIPTYLINE HYDROCHLORIDE
06 1CALCIUM CARBONATE; RISEDRONATE SODIUM
07 1CARBAMAZEPINE
08 6CEFADROXIL/CEFADROXIL HEMIHYDRATE
09 2CHLORTHALIDONE
10 3CLONIDINE HYDROCHLORIDE
11 6CLORAZEPATE DIPOTASSIUM
12 1CYANOCOBALAMIN
13 5DIAZEPAM
14 1DIPHENHYDRAMINE HYDROCHLORIDE
15 3DOPAMINE HYDROCHLORIDE
16 4DOXYCYCLINE HYCLATE
17 1ERYTHROMYCIN
18 1ERYTHROMYCIN STEARATE
19 4ETHINYL ESTRADIOL; NORETHINDRONE
20 1ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
21 2FENOPROFEN CALCIUM
22 2FLURAZEPAM HYDROCHLORIDE
23 4FUROSEMIDE
24 2HYDROCHLOROTHIAZIDE
25 2HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
26 1KANAMYCIN SULFATE
27 2LORAZEPAM
28 1NYSTATIN
29 2OXTRIPHYLLINE
30 1PHENYTOIN SODIUM
31 2PROCAINAMIDE HYDROCHLORIDE
32 1PROPOXYPHENE HYDROCHLORIDE
33 5PROPRANOLOL HYDROCHLORIDE
34 1PYRITHIONE ZINC
35 1QUINIDINE GLUCONATE
36 1QUINIDINE SULFATE
37 1SPIRONOLACTONE
38 7TETRACYCLINE HYDROCHLORIDE
39 1THEOPHYLLINE
40 2VERAPAMIL HYDROCHLORIDE
01 1CAPSULE, DELAYED REL PELLETS;ORAL
02 1CAPSULE, DELAYED RELEASE;ORAL
03 19CAPSULE;ORAL
04 3FOR SUSPENSION;ORAL
05 11INJECTABLE;INJECTION
06 1LOTION;TOPICAL
07 2SOLUTION/DROPS;OTIC
08 1SUPPOSITORY;VAGINAL
09 1SYRUP;ORAL
10 4TABLET, EXTENDED RELEASE;ORAL
11 1TABLET; ORAL
12 45TABLET;ORAL
13 2TABLET;ORAL-21
14 2TABLET;ORAL-28
01 10.005MG;1MG
02 20.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 10.05MG;1MG
04 10.05MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 10.1MG
06 10.2MG
07 10.3%
08 10.3MG
09 1100,000 UNITS
10 1100MG
11 1100MG/ML
12 310MG
13 110MG/ML
14 112.5MG/5ML
15 1120MG
16 1150MG
17 315MG
18 11MG
19 11MG/ML
20 12%
21 12%;1%
22 2200MG
23 220MG
24 6250MG
25 425MG
26 125MG;40MG
27 125MG;80MG
28 22MG
29 23.75MG
30 1300MG;15MG
31 1300MG;30MG
32 1300MG;60MG
33 130MG
34 1330MG
35 1400MG
36 240MG
37 240MG/ML
38 3500MG
39 1500MG/ML
40 350MG
41 150MG/ML
42 15MG
43 25MG/ML
44 1600MG
45 160MG
46 165MG
47 27.5MG
48 175MG
49 380MG
50 180MG/ML
51 3EQ 100MG BASE
52 1EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
53 1EQ 1GM BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
54 1EQ 1GM BASE/3ML
55 1EQ 200MG BASE
56 2EQ 250MG BASE
57 1EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
58 1EQ 2MG BASE
59 1EQ 300MG BASE
60 1EQ 4MG BASE
61 1EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 1EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
63 1EQ 500MG BASE;35MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
64 1EQ 50MG BASE
01 93DISCN
02 1Blank
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 300MG;30MG
Approval Date : 1982-01-01
Application Number : 85218
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;15MG
Approval Date : 1982-01-01
Application Number : 85992
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;60MG
Approval Date : 1982-01-01
Application Number : 87306
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : SOLUTION/DROPS; OTIC
Proprietary Name : ORLEX
Dosage Strength : 2%
Approval Date : 1982-01-01
Application Number : 86845
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETIC ACID, GLACIAL; HYDROCORTISONE
Dosage Form : SOLUTION/DROPS; OTIC
Proprietary Name : ORLEX HC
Dosage Strength : 2%;1%
Approval Date : 1982-01-01
Application Number : 86844
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALBUTEROL SULFATE
Dosage Strength : EQ 2MG BASE
Approval Date : 1990-01-09
Application Number : 72817
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ALBUTEROL SULFATE
Dosage Strength : EQ 4MG BASE
Approval Date : 1990-01-09
Application Number : 72818
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AMITRIL
Dosage Strength : 25MG
Approval Date : 1982-01-01
Application Number : 83937
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AMITRIL
Dosage Strength : 75MG
Approval Date : 1982-01-01
Application Number : 84957
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AMITRIL
Dosage Strength : 150MG
Approval Date : 1982-01-01
Application Number : 86295
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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