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

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01 ALLOPURINOL (3)

02 AZATHIOPRINE SODIUM (1)

03 BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE (1)

04 BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE (1)

05 BISMUTH SUBSALICYLATE; METRONIDAZOLE; TETRACYCLINE HYDROCHLORIDE (1)

06 CAMPHOR (4)

07 CHLORTHALIDONE (2)

08 DIMENHYDRINATE (2)

09 DIPHENYLPYRALINE HYDROCHLORIDE (2)

10 EDETATE CALCIUM DISODIUM (1)

11 ERYTHROMYCIN (1)

12 EUCALYPTOL (2)

13 FLUDROCORTISONE ACETATE (1)

14 GLYCOPYRROLATE (2)

15 GUAIACOL (2)

16 GUAIACOL CARBONATE (4)

17 HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE (1)

18 MECLIZINE HYDROCHLORIDE (4)

19 NITROFURANTOIN (2)

20 NYSTATIN (7)

21 NYSTATIN; TRIAMCINOLONE ACETONIDE (1)

22 OXYTETRACYCLINE HYDROCHLORIDE; POLYMYXIN B SULFATE (1)

23 PENICILLIN G BENZATHINE (1)

24 PROMETHAZINE HYDROCHLORIDE (3)

25 TRIAMCINOLONE (4)

26 TRIAMCINOLONE ACETONIDE (8)

27 TRIAMCINOLONE DIACETATE (1)

28 VITAMIN A PALMITATE (1)

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01 CASPER PHARMA LLC (23)

02 DELCOR ASSET CORP (24)

03 LABORATOIRES CONFAB INC (16)

04 RENAISSANCE PHARMA (1)

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01 CREAM;TOPICAL (4)

02 INJECTABLE;INJECTION (4)

03 LOTION;TOPICAL (4)

04 OINTMENT;OPHTHALMIC (3)

05 OINTMENT;TOPICAL (2)

06 PASTE;DENTAL (1)

07 PASTILLE;ORAL (1)

08 POWDER;TOPICAL (1)

09 SOLUTION;TOPICAL (1)

10 SUPPOSITORY (16)

11 SUSPENSION/DROPS;OTIC (1)

12 SUSPENSION;ORAL (3)

13 SYRUP;ORAL (1)

14 TABLET, CHEWABLE, TABLET, CAPSULE;ORAL (1)

15 TABLET, CHEWABLE;ORAL (1)

16 TABLET;ORAL (19)

17 TABLET;VAGINAL (1)

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01 0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

02 0.1% (1)

03 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (3)

04 0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

05 0.5% (1)

06 0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

07 0.5MG (1)

08 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML (1)

09 1.5MG (1)

10 100,000 UNITS (1)

11 100,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (3)

12 100,000 UNITS/GM;0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons* (1)

13 100,000 UNITS/ML (1)

14 100MG (3)

15 12.5MG (1)

16 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

17 15MG (1)

18 180MG (1)

19 185MG (1)

20 1MG (2)

21 2% (1)

22 200,000 UNITS (1)

23 200MG (3)

24 200MG/ML (1)

25 20MG (1)

26 25MG (3)

27 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

28 25MG/5ML (1)

29 262.4MG,N/A,N/A;N/A,250MG,N/A;N/A,N/A,500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

30 2MG (3)

31 300MG (1)

32 370MG (1)

33 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

34 40MG (1)

35 4MG (1)

36 500,000 UNITS (1)

37 50MG (2)

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

39 50MG/5ML (1)

40 5MG (1)

41 600,000 UNITS/ML (1)

42 600MG (1)

43 8MG (1)

44 90MG (1)

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

46 EQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM (1)

47 EQ 4MG BASE/5ML (1)

48 EQ 50,000 UNITS BASE/ML (1)

49 EQ 5MG BASE/GM;10,000 UNITS/GM (1)

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01 Canada (16)

02 USA (48)

URL Supplier Web Content
TABLET;ORAL
100MG
ZYLOPRIM
USA
16084
1982-01-01
RX
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TABLET;ORAL
300MG
ZYLOPRIM
USA
16084
1982-01-01
RX
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TABLET;ORAL
200MG
ZYLOPRIM
USA
16084
2022-08-04
RX
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INJECTABLE;INJECTION
EQ 100MG BASE/VIAL **F...
IMURAN
USA
17391
1982-01-01
DISCN
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OINTMENT;OPHTHALMIC
400 UNITS/GM;1%;EQ 3.5...
CORTISPORIN
USA
50416
1982-01-01
DISCN
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OINTMENT;OPHTHALMIC
EQ 400 UNITS/GM;EQ 3.5...
LUMI-SPORYN
USA
50417
1982-01-01
RX
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TABLET, CHEWABLE, TABL...
262.4MG,N/A,N/A;N/A,25...
HELIDAC
USA
50719
1996-08-15
DISCN
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SUPPOSITORY
40MG
DEMO-CINEOL ADULTES/AD...
Canada
319716
10
OTC
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SUPPOSITORY
5MG
CREO-RECTAL ADULTES/AD...
Canada
299561
10
OTC
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SUPPOSITORY
2MG
CREO-RECTAL ENFANTS/CH...
Canada
299596
10
OTC
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