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 1Calcium Carbonate
14 1Calcium Carbonate; Cholecalciferol
15 5DIAZEPAM
16 1DIPHENHYDRAMINE HYDROCHLORIDE
17 3DOPAMINE HYDROCHLORIDE
18 4DOXYCYCLINE HYCLATE
19 1ERYTHROMYCIN
20 1ERYTHROMYCIN STEARATE
21 4ETHINYL ESTRADIOL; NORETHINDRONE
22 1ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
23 2FENOPROFEN CALCIUM
24 2FLURAZEPAM HYDROCHLORIDE
25 4FUROSEMIDE
26 2HYDROCHLOROTHIAZIDE
27 2HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
28 1KANAMYCIN SULFATE
29 2LORAZEPAM
30 1NYSTATIN
31 2OXTRIPHYLLINE
32 1PHENYTOIN SODIUM
33 2PROCAINAMIDE HYDROCHLORIDE
34 1PROPOXYPHENE HYDROCHLORIDE
35 5PROPRANOLOL HYDROCHLORIDE
36 1PYRITHIONE ZINC
37 1QUINIDINE GLUCONATE
38 1QUINIDINE SULFATE
39 3Risedronic Acid
40 1SPIRONOLACTONE
41 7TETRACYCLINE HYDROCHLORIDE
42 1THEOPHYLLINE
43 2VERAPAMIL HYDROCHLORIDE
44 3risedronate sodium
45 2testosterone
01 89WARNER CHILCOTT
02 5WARNER CHILCOTT ITALY Srl
03 5WARNER CHILCOTT LLC
04 1Warner Chilcott Deutschland GmbH
05 4Warner Chilcott UK Limited
01 1CAPSULE, DELAYED REL PELLETS;ORAL
02 1CAPSULE, DELAYED RELEASE;ORAL
03 19CAPSULE;ORAL
04 1Calcium Carbonate 1.000Mg 30 Joined' Oral Use
05 1Calcium Carbonate+Cholecalciferol 1.000Mg+880Iu 30 Joined' Oral Use
06 3FILM COATED PILL
07 3FOR SUSPENSION;ORAL
08 11INJECTABLE;INJECTION
09 1LOTION;TOPICAL
10 2SOLUTION/DROPS;OTIC
11 1SUPPOSITORY;VAGINAL
12 1SYRUP;ORAL
13 1Sodium Risedronate 35Mg 4 Units' Oral Use
14 1Sodium Risedronate 5Mg 28 Combined Oral Use
15 1Sodium Risedronate 75Mg 2 Units' Oral Use
16 4TABLET, EXTENDED RELEASE;ORAL
17 1TABLET; ORAL
18 45TABLET;ORAL
19 2TABLET;ORAL-21
20 2TABLET;ORAL-28
21 2TRANSDERMAL PATCH
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02 20.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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04 10.05MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 cpr riv 75 mg
21 12%
22 12%;1%
23 2200MG
24 220MG
25 6250MG
26 425MG
27 125MG;40MG
28 125MG;80MG
29 128 cpr riv 5 mg
30 22MG
31 23.75MG
32 130 bust grat eff 1 g + 880 IU
33 130 cpr eff 1,000 mg bottle
34 2300 MICROGRAMS
35 1300MG;15MG
36 1300MG;30MG
37 1300MG;60MG
38 130MG
39 1330MG
40 135 MG
41 14 cpr riv 35 mg
42 1400MG
43 240MG
44 240MG/ML
45 15 MG
46 3500MG
47 1500MG/ML
48 350MG
49 150MG/ML
50 15MG
51 25MG/ML
52 1600MG
53 160MG
54 165MG
55 27.5MG
56 175 MG
57 175MG
58 380MG
59 180MG/ML
60 3EQ 100MG BASE
61 1EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 1EQ 1GM BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
63 1EQ 1GM BASE/3ML
64 1EQ 200MG BASE
65 2EQ 250MG BASE
66 1EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
67 1EQ 2MG BASE
68 1EQ 300MG BASE
69 1EQ 4MG BASE
70 1EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
71 1EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
72 1EQ 500MG BASE;35MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
73 1EQ 50MG BASE
01 5Italy
02 5Sweden
03 94USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET;ORAL
Brand Name : ACETAMINOPHEN AND CODEINE...
Dosage Strength : 300MG;30MG
Packaging :
Approval Date : 1982-01-01
Application Number : 85218
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET;ORAL
Brand Name : ACETAMINOPHEN AND CODEINE...
Dosage Strength : 300MG;15MG
Packaging :
Approval Date : 1982-01-01
Application Number : 85992
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET;ORAL
Brand Name : ACETAMINOPHEN AND CODEINE...
Dosage Strength : 300MG;60MG
Packaging :
Approval Date : 1982-01-01
Application Number : 87306
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION/DROPS;OTIC
Brand Name : ORLEX
Dosage Strength : 2%
Packaging :
Approval Date : 1982-01-01
Application Number : 86845
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETIC ACID, GLACIAL; HYDROCORTISONE
Dosage Form : SOLUTION/DROPS;OTIC
Brand Name : ORLEX HC
Dosage Strength : 2%;1%
Packaging :
Approval Date : 1982-01-01
Application Number : 86844
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ALBUTEROL SULFATE
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 1990-01-09
Application Number : 72817
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ALBUTEROL SULFATE
Dosage Strength : EQ 4MG BASE
Packaging :
Approval Date : 1990-01-09
Application Number : 72818
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIL
Dosage Strength : 25MG
Packaging :
Approval Date : 1982-01-01
Application Number : 83937
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIL
Dosage Strength : 10MG
Packaging :
Approval Date : 1982-01-01
Application Number : 83939
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIL
Dosage Strength : 150MG
Packaging :
Approval Date : 1982-01-01
Application Number : 86295
Regulatory Info : DISCN
Registration Country : USA
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