01 16AMOXICILLIN
02 13AMOXICILLIN; CLAVULANATE POTASSIUM
03 1LEVOCETIRIZINE DIHYDROCHLORIDE
01 30US ANTIBIOTICS
01 1CAPSULE; ORAL
02 2CAPSULE;ORAL
03 12FOR SUSPENSION;ORAL
04 8TABLET, CHEWABLE;ORAL
05 1TABLET, EXTENDED RELEASE;ORAL
06 6TABLET;ORAL
01 1125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 2125MG/5ML
03 1125MG/5ML;EQ 31.25MG BASE/5ML
04 1125MG;EQ 31.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 11GM;EQ 62.5MG BASE
06 1200MG
07 1200MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 1200MG/5ML;EQ 28.5MG BASE/5ML
09 1200MG;EQ 28.5MG BASE
10 2250MG
11 1250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 2250MG/5ML
13 1250MG/5ML;EQ 62.5MG BASE/5ML
14 1250MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 1250MG;EQ 62.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 1400MG
17 1400MG/5ML
18 1400MG/5ML;EQ 57MG BASE/5ML
19 1400MG;EQ 57MG BASE
20 1500MG
21 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 1500MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 150MG/ML
24 15MG
25 1600MG/5ML;EQ 42.9MG BASE/5ML
26 1875MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 1875MG;EQ 125MG BASE
01 30USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, CHEWABLE;ORAL
Brand Name : AMOXIL
Dosage Strength : 250MG **Federal Regist...
Packaging :
Approval Date : 1982-01-01
Application Number : 50542
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, CHEWABLE;ORAL
Brand Name : AMOXIL
Dosage Strength : 125MG **Federal Regist...
Packaging :
Approval Date : 1982-01-01
Application Number : 50542
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMOXIL
Dosage Strength : 500MG **Federal Regist...
Packaging :
Approval Date : 1998-07-10
Application Number : 50754
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : AMOXIL
Dosage Strength : 400MG/5ML
Packaging :
Approval Date : 1999-04-15
Application Number : 50760
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, CHEWABLE;ORAL
Brand Name : AMOXIL
Dosage Strength : 400MG
Packaging :
Approval Date : 1999-04-15
Application Number : 50761
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : CAPSULE; ORAL
Brand Name : AMOXIL
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number : 62216
Regulatory Info :
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : AMOXIL
Dosage Strength : 125MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62226
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : AMOXIL
Dosage Strength : 250MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62226
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : LAROTID
Dosage Strength : 125MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62226
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : FOR SUSPENSION;ORAL
Brand Name : LAROTID
Dosage Strength : 250MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62226
Regulatory Info : RX
Registration Country : USA
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