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Approved Drug Products of Organon listed in the FDA Orange Book. Original Data : FDA Website

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01 ALENDRONATE SODIUM (5)

02 ALENDRONATE SODIUM; CHOLECALCIFEROL (2)

03 ATORVASTATIN CALCIUM; EZETIMIBE (4)

04 BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE (1)

05 BETAMETHASONE DIPROPIONATE (3)

06 BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE (1)

07 CARBIDOPA; LEVODOPA (5)

08 CLINDAMYCIN PHOSPHATE (1)

09 DESLORATADINE (3)

10 DESLORATADINE; PSEUDOEPHEDRINE SULFATE (2)

11 ETHINYL ESTRADIOL; ETONOGESTREL (1)

12 ETONOGESTREL (2)

13 EZETIMIBE (1)

14 EZETIMIBE; SIMVASTATIN (4)

15 FINASTERIDE (2)

16 FORMOTEROL FUMARATE; MOMETASONE FUROATE (3)

17 GANIRELIX ACETATE (1)

18 HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM (3)

19 LOSARTAN POTASSIUM (3)

20 MIRTAZAPINE (6)

21 MOMETASONE FUROATE (10)

22 MONTELUKAST SODIUM (4)

23 RIZATRIPTAN BENZOATE (4)

24 SIMVASTATIN (5)

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01 AEROSOL, METERED;INHALATION (6)

02 CREAM, AUGMENTED;TOPICAL (1)

03 CREAM;TOPICAL (3)

04 GEL;VAGINAL (1)

05 GRANULE;ORAL (1)

06 IMPLANT;IMPLANTATION (2)

07 INJECTABLE;INJECTION (2)

08 LOTION, AUGMENTED;TOPICAL (1)

09 LOTION;TOPICAL (1)

10 OINTMENT, AUGMENTED;TOPICAL (1)

11 OINTMENT;TOPICAL (1)

12 POWDER;INHALATION (2)

13 RING;VAGINAL (1)

14 SPRAY, METERED;NASAL (1)

15 TABLET, CHEWABLE;ORAL (2)

16 TABLET, EXTENDED RELEASE;ORAL (4)

17 TABLET, ORALLY DISINTEGRATING;ORAL (7)

18 TABLET;ORAL (39)

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01 0.005MG/INH;0.05MG/INH (1)

02 0.005MG/INH;0.1MG/INH (1)

03 0.005MG/INH;0.2MG/INH (1)

04 0.015MG/24HR;0.12MG/24HR (1)

05 0.05MG/INH (1)

06 0.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

07 0.1% (1)

08 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (3)

09 0.10MG/INH (1)

10 0.11MG/INH (1)

11 0.20MG/INH (1)

12 0.22MG/INH (1)

13 100MG (1)

14 10MG (2)

15 10MG;100MG (1)

16 10MG;10MG (1)

17 10MG;20MG (1)

18 10MG;40MG (1)

19 10MG;80MG (1)

20 12.5MG;100MG (1)

21 12.5MG;50MG (1)

22 15MG (2)

23 1MG (1)

24 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

25 2.5MG;120MG (1)

26 20MG (1)

27 250MCG/0.5ML (1)

28 25MG (1)

29 25MG;100MG (2)

30 25MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

31 25MG;250MG (1)

32 30MG (2)

33 3MG/ML;EQ 3MG BASE/ML (1)

34 40MG (1)

35 45MG (1)

36 45MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

37 50MG (1)

38 50MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

39 5MG (3)

40 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

41 5MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

42 68MG/IMPLANT (2)

43 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

44 EQ 0.05% BASE (1)

45 EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

46 EQ 0.05% BASE;1% (1)

47 EQ 10MG BASE (3)

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

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

50 EQ 2% BASE (1)

51 EQ 20MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

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

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

54 EQ 40MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

55 EQ 4MG BASE (1)

56 EQ 4MG BASE/PACKET (1)

57 EQ 5MG BASE (1)

58 EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (3)

59 EQ 70MG BASE (1)

60 EQ 70MG BASE;2,800 IU (1)

61 EQ 70MG BASE;5,600 IU (1)

62 EQ 80MG BASE;10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

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01 DISCN (26)

02 RX (50)

URL Supplier Web Content
TABLET; ORAL
EQ 10MG BASE **Fed...
1995-09-29
20560
FOSAMAX
DISCN
Yes
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TABLET; ORAL
EQ 40MG BASE **Fed...
1995-09-29
20560
FOSAMAX
DISCN
Yes
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TABLET; ORAL
EQ 5MG BASE **Fede...
1997-04-25
20560
FOSAMAX
DISCN
Yes
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TABLET; ORAL
EQ 35MG BASE **Fed...
2000-10-20
20560
FOSAMAX
DISCN
Yes
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TABLET; ORAL
EQ 70MG BASE
2000-10-20
20560
FOSAMAX
RX
Yes
AB
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TABLET; ORAL
EQ 70MG BASE;2,800...
2005-04-07
21762
FOSAMAX PLUS D
RX
Yes
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TABLET; ORAL
EQ 70MG BASE;5,600...
2007-04-26
21762
FOSAMAX PLUS D
RX
Yes
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TABLET; ORAL
EQ 10MG BASE;10MG ...
2013-05-03
200153
LIPTRUZET
DISCN
Yes
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TABLET; ORAL
EQ 20MG BASE;10MG ...
2013-05-03
200153
LIPTRUZET
DISCN
Yes
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TABLET; ORAL
EQ 40MG BASE;10MG ...
2013-05-03
200153
LIPTRUZET
DISCN
Yes
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