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Approved Drug Products containing Cefadroxil listed in the FDA Orange Book. Original Data : FDA Website

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01 ANI PHARMS (5)

02 APOTHECON (4)

03 AUROBINDO (2)

04 AUROBINDO PHARMA (1)

05 BRISTOL (5)

06 CHARTWELL RX (4)

07 CSPC OUYI (1)

08 HIKMA (2)

09 HIKMA PHARMS (2)

10 IVAX SUB TEVA PHARMS (1)

11 LUPIN (3)

12 PUREPAC PHARM (1)

13 RANBAXY (1)

14 RANBAXY LABS LTD (1)

15 SANDOZ (1)

16 SUN PHARM INDS LTD (3)

17 TEVA (1)

18 TEVA PHARMS (2)

19 WARNER CHILCOTT (6)

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01 CAPSULE;ORAL (14)

02 FOR SUSPENSION;ORAL (25)

03 TABLET;ORAL (7)

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01 DISCN (38)

02 RX (8)

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01 CEFADROXIL (34)

02 DURICEF (6)

03 ULTRACEF (6)

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01 No (41)

02 Yes (5)

URL Supplier Web Content
FOR SUSPENSION;ORAL
EQ 125MG BASE/5ML
1982-01-01
62334
CEFADROXIL
DISCN
No
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FOR SUSPENSION;ORAL
EQ 250MG BASE/5ML
1982-01-01
62334
CEFADROXIL
DISCN
No
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FOR SUSPENSION;ORAL
EQ 500MG BASE/5ML
1982-01-01
62334
CEFADROXIL
DISCN
No
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CAPSULE;ORAL
EQ 500MG BASE
1982-01-01
62291
CEFADROXIL
DISCN
No
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CAPSULE;ORAL
EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-01-01
50512
DURICEF
DISCN
Yes
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CAPSULE;ORAL
EQ 250MG BASE
1982-01-01
50512
DURICEF
DISCN
No
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FOR SUSPENSION;ORAL
EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-01-01
50527
DURICEF
DISCN
Yes
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FOR SUSPENSION;ORAL
EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-01-01
50527
DURICEF
DISCN
Yes
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FOR SUSPENSION;ORAL
EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-01-01
50527
DURICEF
DISCN
Yes
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TABLET;ORAL
EQ 1GM BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-01-01
50528
DURICEF
DISCN
Yes
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