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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 050655

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NALLPEN IN PLASTIC CONTAINER (NAFCILLIN SODIUM)
EQ 20MG BASE/ML
Marketing Status: Prescription
Active Ingredient: NAFCILLIN SODIUM
Proprietary Name: NALLPEN IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 20MG BASE/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N050655
Product Number: 001
Approval Date: Oct 31, 1989
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
NALLPEN IN PLASTIC CONTAINER (NAFCILLIN SODIUM)
EQ 2GM BASE/100ML
Marketing Status: Prescription
Active Ingredient: NAFCILLIN SODIUM
Proprietary Name: NALLPEN IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N050655
Product Number: 002
Approval Date: Oct 31, 1989
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
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