Details for New Drug Application (NDA): 065115
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The generic ingredient in CEFADROXIL is cefadroxil/cefadroxil hemihydrate. Twenty-two suppliers are listed for this compound. Additional details are available on the cefadroxil/cefadroxil hemihydrate profile page.
Summary for 065115
Tradename: | CEFADROXIL |
Applicant: | Sun Pharm Inds Ltd |
Ingredient: | cefadroxil/cefadroxil hemihydrate |
Patents: | 0 |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | FOR SUSPENSION;ORAL | Strength | EQ 125MG BASE/5ML | ||||
Approval Date: | Mar 26, 2003 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | FOR SUSPENSION;ORAL | Strength | EQ 250MG BASE/5ML | ||||
Approval Date: | Mar 26, 2003 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | FOR SUSPENSION;ORAL | Strength | EQ 500MG BASE/5ML | ||||
Approval Date: | Mar 26, 2003 | TE: | RLD: | No |
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