Product Details for ANDA 062719
AMPICILLIN SODIUM (AMPICILLIN SODIUM)
EQ 250MG BASE/VIAL
Marketing Status: Prescription
EQ 500MG BASE/VIAL
Marketing Status: Prescription
EQ 1GM BASE/VIAL
Marketing Status: Prescription
EQ 250MG BASE/VIAL
Marketing Status: Prescription
Active Ingredient: AMPICILLIN SODIUM
Proprietary Name: AMPICILLIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 250MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A062719
Product Number: 001
Approval Date: May 12, 1987
Applicant Holder Full Name: ISTITUTO BIOCHIMICO ITALIANO SPA
Marketing Status: Prescription
Patent and Exclusivity Information
AMPICILLIN SODIUM (AMPICILLIN SODIUM)
Proprietary Name: AMPICILLIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 250MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A062719
Product Number: 001
Approval Date: May 12, 1987
Applicant Holder Full Name: ISTITUTO BIOCHIMICO ITALIANO SPA
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 500MG BASE/VIAL
Marketing Status: Prescription
Active Ingredient: AMPICILLIN SODIUM
Proprietary Name: AMPICILLIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A062719
Product Number: 003
Approval Date: May 12, 1987
Applicant Holder Full Name: ISTITUTO BIOCHIMICO ITALIANO SPA
Marketing Status: Prescription
Patent and Exclusivity Information
AMPICILLIN SODIUM (AMPICILLIN SODIUM)
Proprietary Name: AMPICILLIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A062719
Product Number: 003
Approval Date: May 12, 1987
Applicant Holder Full Name: ISTITUTO BIOCHIMICO ITALIANO SPA
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 1GM BASE/VIAL
Marketing Status: Prescription
Active Ingredient: AMPICILLIN SODIUM
Proprietary Name: AMPICILLIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A062719
Product Number: 002
Approval Date: May 12, 1987
Applicant Holder Full Name: ISTITUTO BIOCHIMICO ITALIANO SPA
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: AMPICILLIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A062719
Product Number: 002
Approval Date: May 12, 1987
Applicant Holder Full Name: ISTITUTO BIOCHIMICO ITALIANO SPA
Marketing Status: Prescription
Patent and Exclusivity Information