01 15AMOXICILLIN
02 13AMOXICILLIN; CLAVULANATE POTASSIUM
03 1LEVOCETIRIZINE DIHYDROCHLORIDE
01 2CAPSULE;ORAL
02 12FOR SUSPENSION;ORAL
03 8TABLET, CHEWABLE;ORAL
04 1TABLET, EXTENDED RELEASE;ORAL
05 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01 1125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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04 1125MG;EQ 31.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 11GM;EQ 62.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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07 1200MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 1200MG/5ML;EQ 28.5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 1200MG;EQ 28.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1250MG
11 1250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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14 1250MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 1250MG;EQ 62.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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18 1400MG/5ML;EQ 57MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 1400MG;EQ 57MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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21 1500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 1500MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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26 1875MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 17DISCN
02 12RX
RLD : Yes
TE Code :
Dosage Form : TABLET, CHEWABLE; ORAL
Proprietary Name : AMOXIL
Dosage Strength : 250MG **Federal Register...
Approval Date : 1982-01-01
Application Number : 50542
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, CHEWABLE; ORAL
Proprietary Name : AMOXIL
Dosage Strength : 125MG **Federal Register...
Approval Date : 1982-01-01
Application Number : 50542
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AMOXIL
Dosage Strength : 875MG **Federal Register...
Approval Date : 1998-07-10
Application Number : 50754
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : AMOXIL
Dosage Strength : 250MG
Approval Date : 1982-01-01
Application Number : 62216
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : AMOXIL
Dosage Strength : 500MG
Approval Date : 1982-01-01
Application Number : 62216
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : AMOXIL
Dosage Strength : 125MG/5ML
Approval Date : 1982-01-01
Application Number : 62226
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : AMOXIL
Dosage Strength : 250MG/5ML
Approval Date : 1982-01-01
Application Number : 62226
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : LAROTID
Dosage Strength : 125MG/5ML
Approval Date : 1982-01-01
Application Number : 62226
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : LAROTID
Dosage Strength : 250MG/5ML
Approval Date : 1982-01-01
Application Number : 62226
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : AMOXIL
Dosage Strength : 50MG/ML
Approval Date : 1982-01-01
Application Number : 62226
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
