01 5ANI PHARMS
02 4APOTHECON
03 2AUROBINDO
04 1AUROBINDO PHARMA
05 5BRISTOL
06 4CHARTWELL RX
07 1CSPC OUYI
08 2HIKMA
09 2HIKMA PHARMS
10 1IVAX SUB TEVA PHARMS
11 3LUPIN
12 1PUREPAC PHARM
13 1RANBAXY
14 1RANBAXY LABS LTD
15 1SANDOZ
16 3SUN PHARM INDS LTD
17 1TEVA
18 2TEVA PHARMS
19 6WARNER CHILCOTT
01 14CAPSULE;ORAL
02 25FOR SUSPENSION;ORAL
03 7TABLET;ORAL
01 38DISCN
02 8RX
01 34CEFADROXIL
02 6DURICEF
03 6ULTRACEF
01 41No
02 5Yes
RLD : No
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 62334
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 62334
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 500MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 62334
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : CEFADROXIL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 1982-01-01
Application Number : 62291
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50512
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 1982-01-01
Application Number : 50512
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50527
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50527
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50527
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Brand Name : DURICEF
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1GM BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50528
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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