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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 062226

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AMOXIL (AMOXICILLIN)
50MG/ML
Marketing Status: Prescription
Active Ingredient: AMOXICILLIN
Proprietary Name: AMOXIL
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 50MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A062226
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: US ANTIBIOTICS LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
AMOXIL (AMOXICILLIN)
125MG/5ML
Marketing Status: Prescription
Active Ingredient: AMOXICILLIN
Proprietary Name: AMOXIL
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 125MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A062226
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: US ANTIBIOTICS LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
AMOXIL (AMOXICILLIN)
250MG/5ML
Marketing Status: Prescription
Active Ingredient: AMOXICILLIN
Proprietary Name: AMOXIL
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 250MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A062226
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: US ANTIBIOTICS LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
LAROTID (AMOXICILLIN)
125MG/5ML
Marketing Status: Prescription
Active Ingredient: AMOXICILLIN
Proprietary Name: LAROTID
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 125MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A062226
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: US ANTIBIOTICS LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
LAROTID (AMOXICILLIN)
250MG/5ML
Marketing Status: Prescription
Active Ingredient: AMOXICILLIN
Proprietary Name: LAROTID
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 250MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A062226
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: US ANTIBIOTICS LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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