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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 062991

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PENICILLIN G POTASSIUM (PENICILLIN G POTASSIUM)
1,000,000 UNITS/VIAL
Marketing Status: Discontinued
Active Ingredient: PENICILLIN G POTASSIUM
Proprietary Name: PENICILLIN G POTASSIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1,000,000 UNITS/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A062991
Product Number: 001
Approval Date: Sep 13, 1988
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
PENICILLIN G POTASSIUM (PENICILLIN G POTASSIUM)
5,000,000 UNITS/VIAL
Marketing Status: Discontinued
Active Ingredient: PENICILLIN G POTASSIUM
Proprietary Name: PENICILLIN G POTASSIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5,000,000 UNITS/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A062991
Product Number: 002
Approval Date: Sep 13, 1988
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
PENICILLIN G POTASSIUM (PENICILLIN G POTASSIUM)
10,000,000 UNITS/VIAL
Marketing Status: Discontinued
Active Ingredient: PENICILLIN G POTASSIUM
Proprietary Name: PENICILLIN G POTASSIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10,000,000 UNITS/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A062991
Product Number: 003
Approval Date: Sep 13, 1988
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
PENICILLIN G POTASSIUM (PENICILLIN G POTASSIUM)
20,000,000 UNITS/VIAL
Marketing Status: Discontinued
Active Ingredient: PENICILLIN G POTASSIUM
Proprietary Name: PENICILLIN G POTASSIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20,000,000 UNITS/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A062991
Product Number: 004
Approval Date: Sep 13, 1988
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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