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 2Calcium Carbonate; Cholecalciferol
15 2Calcium Carbonate; Cholecalciferol; Risedronate Sodium
16 1Calcium Carbonate; Risedronate Sodium
17 5DIAZEPAM
18 1DIPHENHYDRAMINE HYDROCHLORIDE
19 3DOPAMINE HYDROCHLORIDE
20 4DOXYCYCLINE HYCLATE
21 1ERYTHROMYCIN
22 1ERYTHROMYCIN STEARATE
23 4ETHINYL ESTRADIOL; NORETHINDRONE
24 1ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
25 1Etidronate Disodium
26 1Etidronate Disodium; Calcium Carbonate
27 2FENOPROFEN CALCIUM
28 2FLURAZEPAM HYDROCHLORIDE
29 4FUROSEMIDE
30 2HYDROCHLOROTHIAZIDE
31 2HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
32 1KANAMYCIN SULFATE
33 2LORAZEPAM
34 1NYSTATIN
35 2OXTRIPHYLLINE
36 1PHENYTOIN SODIUM
37 2PROCAINAMIDE HYDROCHLORIDE
38 1PROPOXYPHENE HYDROCHLORIDE
39 5PROPRANOLOL HYDROCHLORIDE
40 1PYRITHIONE ZINC
41 1QUINIDINE GLUCONATE
42 1QUINIDINE SULFATE
43 1Risedronate Sodium
44 3Risedronic Acid
45 1SPIRONOLACTONE
46 7TETRACYCLINE HYDROCHLORIDE
47 1THEOPHYLLINE
48 2Testosteron
49 2VERAPAMIL HYDROCHLORIDE
01 89WARNER CHILCOTT
02 5WARNER CHILCOTT ITALY Srl
03 5WARNER CHILCOTT LLC
04 1Warner Chilcott Deutschland Gmbh
05 1Warner Chilcott Italy Srl
06 7Warner 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 1Effervescent Granule
07 3FOR SUSPENSION;ORAL
08 4Film Coated Tablet
09 11INJECTABLE;INJECTION
10 1LOTION;TOPICAL
11 2SOLUTION/DROPS;OTIC
12 1SUPPOSITORY;VAGINAL
13 1SYRUP;ORAL
14 1Sodium Risedronate 35Mg 4 Units' Oral Use
15 1Sodium Risedronate 5Mg 28 Combined Oral Use
16 1Sodium Risedronate 75Mg 2 Units' Oral Use
17 4TABLET, EXTENDED RELEASE;ORAL
18 1TABLET; ORAL
19 45TABLET;ORAL
20 2TABLET;ORAL-21
21 2TABLET;ORAL-28
22 2Tablet
23 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02 20.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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04 10.05MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 11000MG; 880 IU
11 1100MG
12 1100MG/ML
13 310MG
14 110MG/ML
15 112.5MG/5ML
16 1120MG
17 1150MG
18 315MG
19 11MG
20 11MG/ML
21 12 cpr riv 75 mg
22 12%
23 12%;1%
24 2200MG
25 1200mg
26 220MG
27 6250MG
28 425MG
29 125MG;40MG
30 125MG;80MG
31 128 cpr riv 5 mg
32 22MG
33 23.75MG
34 130 bust grat eff 1 g + 880 IU
35 130 cpr eff 1,000 mg bottle
36 1300MG;15MG
37 1300MG;30MG
38 1300MG;60MG
39 2300mcg/24hours
40 130MG
41 130mg
42 1330MG
43 135mg;1000mg;880IE
44 135mg;500mg;400IU
45 14 cpr riv 35 mg
46 1400MG
47 1400mg;500mg
48 240MG
49 240MG/ML
50 3500MG
51 1500MG/ML
52 350MG
53 150MG/ML
54 15MG
55 25MG/ML
56 1600MG
57 160MG
58 165MG
59 27.5MG
60 175MG
61 380MG
62 180MG/ML
63 3EQ 100MG BASE
64 1EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
65 1EQ 1GM BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
66 1EQ 1GM BASE/3ML
67 1EQ 200MG BASE
68 2EQ 250MG BASE
69 1EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 1EQ 2MG BASE
71 1EQ 300MG BASE
72 1EQ 4MG BASE
73 1EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
74 1EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
75 1EQ 500MG BASE;35MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
76 1EQ 50MG BASE
77 1Blank
01 5Italy
02 1Spain
03 8Sweden
04 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 : 50MG
Packaging :
Approval Date : 1982-01-01
Application Number : 83938
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
