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Wyeth Pharmaceuticals Inc's list of EU CTD Dossiers, Marketing Authorizations, In, Out Licensing Opportunities & Finished Dosage Formulations aggregated by PharmaCompass

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01 AMIODARONE HYDROCHLORIDE (2)

02 AMOXICILLIN (4)

03 AMPICILLIN SODIUM (16)

04 AMPICILLIN/AMPICILLIN TRIHYDRATE (11)

05 ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE (3)

06 BAZEDOXIFENE ACETATE; ESTROGENS, CONJUGATED (1)

07 BROMPHENIRAMINE MALEATE (4)

08 CARPHENAZINE MALEATE (4)

09 CEFPIRAMIDE SODIUM (3)

10 CHLORPROMAZINE HYDROCHLORIDE (1)

11 CLOFIBRATE (1)

12 CONJUGATED ESTROGENS/MEDROXYPROGESTERONE ACETATE (1)

13 CYANOCOBALAMIN (2)

14 CYCLACILLIN (5)

15 Calcium Levofolinate (3)

16 Chlortetracycline (2)

17 Conjugated Estrogens (2)

18 Conjugated Estrogens; Medroxyprogesterone Acetate (3)

19 DAUNORUBICIN HYDROCHLORIDE (1)

20 DEXAMETHASONE SODIUM PHOSPHATE (1)

21 DICLOXACILLIN SODIUM (3)

22 DIGOXIN (1)

23 DIMENHYDRINATE (1)

24 DIPHENHYDRAMINE HYDROCHLORIDE (1)

25 EPINEPHRINE (1)

26 EPINEPHRINE BITARTRATE (1)

27 ERYTHROMYCIN ETHYLSUCCINATE (2)

28 ERYTHROMYCIN STEARATE (2)

29 ESTROGENS, CONJUGATED (10)

30 ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE (7)

31 ESTROGENS, CONJUGATED; MEPROBAMATE (2)

32 ESTRONE (1)

33 ETHINYL ESTRADIOL; LEVONORGESTREL (3)

34 ETHINYL ESTRADIOL; NORGESTREL (3)

35 ETHIONAMIDE (1)

36 ETODOLAC (7)

37 Ethinyl Estradiol; Gestodene (2)

38 Ethinyl Estradiol; Levonorgestrel (2)

39 Ethinylestradiol (1)

40 FOLIC ACID (2)

41 FUROSEMIDE (1)

42 GEMTUZUMAB OZOGAMICIN (1)

43 GENTAMICIN SULFATE (2)

44 GRISEOFULVIN, MICROCRYSTALLINE (3)

45 GRISEOFULVIN, ULTRAMICROCRYSTALLINE (4)

46 GUANABENZ ACETATE (3)

47 HALOTHANE (1)

48 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE (5)

49 HYDROFLUMETHIAZIDE (1)

50 HYDROXYZINE HYDROCHLORIDE (2)

51 INOTUZUMAB OZOGAMICIN (1)

52 ISOSORBIDE DINITRATE (2)

53 KETOPROFEN (7)

54 LEVONORGESTREL (2)

55 LIDOCAINE HYDROCHLORIDE (2)

56 Levonorgestrel (1)

57 Lorazepam (5)

58 MAZINDOL (2)

59 MEPERIDINE HYDROCHLORIDE (1)

60 MEPROBAMATE (3)

61 NAFCILLIN SODIUM (12)

62 NALOXONE HYDROCHLORIDE (4)

63 PANTOPRAZOLE SODIUM (4)

64 PENICILLIN G BENZATHINE (3)

65 PENICILLIN G POTASSIUM (3)

66 PENICILLIN V POTASSIUM (5)

67 PENTAGASTRIN (1)

68 PENTOBARBITAL SODIUM (2)

69 PENTOLINIUM TARTRATE (1)

70 PHENDIMETRAZINE TARTRATE (1)

71 PIPERACILLIN SODIUM (7)

72 PIPERACILLIN SODIUM; TAZOBACTAM SODIUM (4)

73 POLYESTRADIOL PHOSPHATE (1)

74 PRALIDOXIME CHLORIDE (1)

75 PROCHLORPERAZINE EDISYLATE (1)

76 PROMAZINE HYDROCHLORIDE (8)

77 PROMETHAZINE HYDROCHLORIDE (2)

78 PROPRANOLOL HYDROCHLORIDE (7)

79 Pseudoephedrine HCl (1)

80 QUINIDINE SULFATE (1)

81 SECOBARBITAL SODIUM (2)

82 SULFAMETHIZOLE (2)

83 Streptococcus Pneumoniae Serotype 4 (1)

84 Suncholin (2)

85 TETRACYCLINE HYDROCHLORIDE (4)

86 THIAMINE HYDROCHLORIDE (1)

87 TRISULFAPYRIMIDINES (SULFADIAZINE;SULFAMERAZINE;SULFAMETHAZINE) (2)

88 Tazobactam (1)

89 VENLAFAXINE HYDROCHLORIDE (6)

90 kalciumlevofolinatpentahydrat (1)

91 lansoprazole (4)

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01 WYETH AYERST (157)

02 WYETH CONS (6)

03 WYETH LEDERLE SpA (21)

04 WYETH PHARMS (34)

05 WYETH PHARMS INC (39)

06 Wyeth AB (3)

07 Wyeth Consumer Healthcare (5)

08 Wyeth Lederle Nordic AB (2)

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01 AEROSOL, METERED;INHALATION (2)

02 CAPSULE, EXTENDED RELEASE;ORAL (7)

03 CAPSULE;ORAL (24)

04 CONCENTRATE;ORAL (3)

05 CREAM;TOPICAL, VAGINAL (1)

06 FOR SOLUTION;ORAL (3)

07 FOR SUSPENSION, DELAYED RELEASE;ORAL (1)

08 FOR SUSPENSION;ORAL (13)

09 GASTRO-RESISTANT CAPSULE, HARD (2)

10 GRANULES FOR ORAL SUSPENSION (2)

11 IMPLANT;IMPLANTATION (2)

12 INJ (3)

13 INJECTABLE;INJECTION (76)

14 INJECTABLE;INTRAVENOUS (1)

15 LIQUID;INHALATION (1)

16 POWDER, FOR INJECTION SOLUTION, LYOPHILIZED POWDER (1)

17 SUSPENSION;ORAL (5)

18 SYRUP;ORAL (1)

19 TAB (2)

20 TABLET (1)

21 TABLET, DELAYED RELEASE;ORAL (2)

22 TABLET, EXTENDED RELEASE;ORAL (7)

23 TABLET; ORAL (2)

24 TABLET;ORAL (70)

25 TABLET;ORAL-21 (2)

26 TABLET;ORAL-28 (10)

27 Tablet; Oral (1)

28 VIAL;SINGLE-DOSE (1)

29 Blank (21)

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01 0.02MG/ML (2)

02 0.02MG;0.09MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

03 0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

04 0.03MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

05 0.05MG;0.5MG (2)

06 0.1MG/ML (1)

07 0.25MG/ML (1)

08 0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

09 0.2MG/INH (1)

10 0.3MG (2)

11 0.3MG/INH (1)

12 0.3MG;1.5MG (1)

13 0.45MG (2)

14 0.45MG/1.5MG & 0.3MG/1.5MG (1)

15 0.45MG;1.5MG (1)

16 0.45MG;200MG (1)

17 0.45MG;400MG (1)

18 0.4MG/ML (2)

19 0.4MG/ML;100MG/ML (1)

20 0.4MG/ML;50MG/ML (1)

21 0.4MG/ML;75MG/ML (1)

22 0.625MG (1)

23 0.625MG,0.625MG;2.5MG,2.5MG (1)

24 0.625MG,0.625MG;N/A,5MG (2)

25 0.625MG/GM (1)

26 0.625MG;2.5MG (1)

27 0.625MG;5MG (1)

28 0.9/MG/VIAL (1)

29 0.9MG (1)

30 1 Bottle Iv 25 Mg   (1)

31 1% (1)

32 1.25MG (1)

33 10 Cpr 7.5 Mg   (1)

34 100MG (3)

35 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

36 100MG/ML (3)

37 10MG (1)

38 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

39 10MG/5ML (1)

40 10MG/ML (4)

41 12.5MG (1)

42 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

43 125MG (2)

44 125MG/5ML (3)

45 12MG (1)

46 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

47 15MG (2)

48 165MG (1)

49 167MG/5ML;167MG/5ML;167MG/5ML (1)

50 167MG;167MG;167MG (1)

51 1MG (1)

52 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

53 1MG/ML (1)

54 2% (1)

55 2.5MG (1)

56 20 Bust Grat 2.5 Mg   (1)

57 20 Cpr 1 Mg   (1)

58 20 Cpr 2.5 Mg   (1)

59 20 Cpr Orodispers 2.5 Mg   (1)

60 20 Orodispers Cpr 1 Mg   (1)

61 200,000 UNITS (2)

62 200MG (2)

63 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (3)

64 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

65 21 Cpr Riv 0.075 Mg + 0.02 Mg   (1)

66 21 Cpr Riv 0.25 Mg + 0.10 Mg   (1)

67 21 Cpr Riv 100 Mcg + 20 Mcg   (1)

68 250,000 UNITS (1)

69 250MG (9)

70 250MG/5ML (3)

71 25MG (2)

72 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

73 25MG/ML (3)

74 25MG/VIAL (1)

75 25MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

76 25MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

77 28 Cpr 0.3 Mg   (1)

78 28 Cpr 1.25 Mg   (1)

79 28 Cpr Riv 0.30 Mg + 1.5 Mg (1)

80 28 Cpr Riv 0.625 Mg + 2.5 Mg   (1)

81 28 Cpr Riv 0.625 Mg + 5 Mg   (1)

82 28 Cpr Riv 60 Mcg + 15 Mcg   (1)

83 2MG (1)

84 2MG/ML (1)

85 2mcg/0.5ml (2)

86 3 Ampoules Im Ev 1,000 Mg/4 Ml   (1)

87 30 MG (2)

88 300,000 UNITS/5ML (1)

89 300,000 UNITS/ML (1)

90 300MG (2)

91 30MG/ML (1)

92 30mg (3)

93 330MG (1)

94 35MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

95 36MG/IMPLANT (1)

96 4.5MG (1)

97 400,000 UNITS (1)

98 400MG (2)

99 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

100 40MG (2)

101 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

102 40MG/AMP (1)

103 4MG (1)

104 5 Ampoules Im Ev 500 Mg/4 Ml   (1)

105 500MG (9)

106 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

107 500MG/5ML (2)

108 50MG (4)

109 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

110 50MG/ML (7)

111 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

112 50MG;120MG (1)

113 50MG;160MG (1)

114 50MG;80MG (1)

115 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

116 600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

117 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

118 7.5 MG (1)

119 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

120 75MG/IMPLANT (1)

121 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

122 8MG (1)

123 90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

124 99.99% (1)

125 Cream Oftalm 3,5 G 1%   (1)

126 EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

127 EQ 100MG BASE/ML (1)

128 EQ 10GM BASE/VIAL (1)

129 EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

130 EQ 10MG BASE/ML (1)

131 EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

132 EQ 125MG BASE (1)

133 EQ 125MG BASE/5ML (2)

134 EQ 125MG BASE/VIAL (2)

135 EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

136 EQ 16MG BASE (1)

137 EQ 1GM BASE/VIAL (3)

138 EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (3)

139 EQ 200MG BASE/5ML (1)

140 EQ 20GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

141 EQ 20MG BASE (1)

142 EQ 20MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

143 EQ 20MG BASE;0.45MG (1)

144 EQ 250MG BASE (4)

145 EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

146 EQ 250MG BASE/5ML (3)

147 EQ 250MG BASE/VIAL (2)

148 EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

149 EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

150 EQ 2GM BASE/VIAL (4)

151 EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (4)

152 EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

153 EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

154 EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

155 EQ 3GM BASE/VIAL (1)

156 EQ 3GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

157 EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

158 EQ 400MG BASE/5ML (1)

159 EQ 40GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

160 EQ 40MG BASE (2)

161 EQ 40MG BASE/ML (1)

162 EQ 40MG BASE/VIAL (1)

163 EQ 4GM BASE/VIAL (1)

164 EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (3)

165 EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

166 EQ 4MG BASE (1)

167 EQ 4MG PHOSPHATE/ML (1)

168 EQ 500MG BASE (4)

169 EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

170 EQ 500MG BASE/VIAL (2)

171 EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (3)

172 EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

173 EQ 5MG BASE/ML (1)

174 EQ 62.5MG BASE/5ML (1)

175 EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

176 EQ 8MG BASE (1)

177 Gtt Os 10 Ml 2 Mg/Ml   (1)

178 Ung Derm 14.2 G 3%   (1)

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01 Italy (21)

02 South Africa (5)

03 Sweden (5)

04 USA (236)

URL Supplier Web Content
TABLET;ORAL
200MG **Federal Regist...
CORDARONE
USA
18972
1985-12-24
DISCN
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INJECTABLE;INJECTION
50MG/ML **Federal Regi...
CORDARONE
USA
20377
1995-08-03
DISCN
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CAPSULE;ORAL
250MG
WYMOX
USA
62120
1982-01-01
DISCN
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CAPSULE;ORAL
500MG
WYMOX
USA
62120
1982-01-01
DISCN
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FOR SUSPENSION;ORAL
125MG/5ML
WYMOX
USA
62131
1982-01-01
DISCN
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FOR SUSPENSION;ORAL
250MG/5ML
WYMOX
USA
62131
1982-01-01
DISCN
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INJECTABLE;INJECTION
EQ 125MG BASE/VIAL **F...
PENBRITIN-S
USA
50072
1982-01-01
DISCN
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INJECTABLE;INJECTION
EQ 500MG BASE/VIAL **F...
PENBRITIN-S
USA
50072
1982-01-01
DISCN
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INJECTABLE;INJECTION
EQ 500MG BASE/VIAL
OMNIPEN-N
USA
60626
1982-01-01
DISCN
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INJECTABLE;INJECTION
EQ 500MG BASE/VIAL
OMNIPEN-N
USA
62718
1986-12-16
DISCN
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