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

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01 AMOXICILLIN (16)

02 AMOXICILLIN; CLAVULANATE POTASSIUM (13)

03 LEVOCETIRIZINE DIHYDROCHLORIDE (1)

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01 US ANTIBIOTICS (30)

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01 CAPSULE; ORAL (1)

02 CAPSULE;ORAL (2)

03 FOR SUSPENSION;ORAL (12)

04 TABLET, CHEWABLE;ORAL (8)

05 TABLET, EXTENDED RELEASE;ORAL (1)

06 TABLET;ORAL (6)

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01 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

02 125MG/5ML (2)

03 125MG/5ML;EQ 31.25MG BASE/5ML (1)

04 125MG;EQ 31.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

05 1GM;EQ 62.5MG BASE (1)

06 200MG (1)

07 200MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

08 200MG/5ML;EQ 28.5MG BASE/5ML (1)

09 200MG;EQ 28.5MG BASE (1)

10 250MG (2)

11 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

12 250MG/5ML (2)

13 250MG/5ML;EQ 62.5MG BASE/5ML (1)

14 250MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

15 250MG;EQ 62.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

16 400MG (1)

17 400MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

18 400MG/5ML;EQ 57MG BASE/5ML (1)

19 400MG;EQ 57MG BASE (1)

20 500MG (1)

21 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

22 500MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

23 50MG/ML (1)

24 5MG (1)

25 600MG/5ML;EQ 42.9MG BASE/5ML (1)

26 875MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

27 875MG;EQ 125MG BASE (1)

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01 USA (30)

URL Supplier Web Content
TABLET, CHEWABLE;ORAL
125MG **Federal Regist...
AMOXIL
USA
50542
1982-01-01
DISCN
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TABLET;ORAL
500MG **Federal Regist...
AMOXIL
USA
50754
1998-07-10
DISCN
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FOR SUSPENSION;ORAL
200MG/5ML **Federal Re...
AMOXIL
USA
50760
1999-04-15
DISCN
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TABLET, CHEWABLE;ORAL
200MG
AMOXIL
USA
50761
1999-04-15
DISCN
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URL Supplier Web Content
CAPSULE;ORAL
250MG
AMOXIL
USA
62216
1982-01-01
RX
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URL Supplier Web Content
CAPSULE;ORAL
500MG
AMOXIL
USA
62216
1982-01-01
RX
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URL Supplier Web Content
FOR SUSPENSION;ORAL
250MG/5ML
AMOXIL
USA
62226
1982-01-01
RX
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FOR SUSPENSION;ORAL
125MG/5ML
LAROTID
USA
62226
1982-01-01
RX
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FOR SUSPENSION;ORAL
250MG/5ML
LAROTID
USA
62226
1982-01-01
RX
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FOR SUSPENSION;ORAL
50MG/ML
AMOXIL
USA
62226
1982-01-01
RX
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