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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050308

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POLYCILLIN (AMPICILLIN/AMPICILLIN TRIHYDRATE)
EQ 100MG BASE/ML
Marketing Status: Discontinued
Active Ingredient: AMPICILLIN/AMPICILLIN TRIHYDRATE
Proprietary Name: POLYCILLIN
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: EQ 100MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050308
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BRISTOL LABORATORIES INC DIV BRISTOL MYERS CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
POLYCILLIN (AMPICILLIN/AMPICILLIN TRIHYDRATE)
EQ 125MG BASE/5ML
Marketing Status: Discontinued
Active Ingredient: AMPICILLIN/AMPICILLIN TRIHYDRATE
Proprietary Name: POLYCILLIN
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: EQ 125MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050308
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BRISTOL LABORATORIES INC DIV BRISTOL MYERS CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
POLYCILLIN (AMPICILLIN/AMPICILLIN TRIHYDRATE)
EQ 250MG BASE/5ML
Marketing Status: Discontinued
Active Ingredient: AMPICILLIN/AMPICILLIN TRIHYDRATE
Proprietary Name: POLYCILLIN
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: EQ 250MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050308
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BRISTOL LABORATORIES INC DIV BRISTOL MYERS CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
POLYCILLIN (AMPICILLIN/AMPICILLIN TRIHYDRATE)
EQ 500MG BASE/5ML
Marketing Status: Discontinued
Active Ingredient: AMPICILLIN/AMPICILLIN TRIHYDRATE
Proprietary Name: POLYCILLIN
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: EQ 500MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N050308
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BRISTOL LABORATORIES INC DIV BRISTOL MYERS CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
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