Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019952

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HEPARIN SODIUM 20,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER (HEPARIN SODIUM)
4,000 UNITS/100ML
Marketing Status: Prescription

Active Ingredient: HEPARIN SODIUM
Proprietary Name: HEPARIN SODIUM 20,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 4,000 UNITS/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N019952
Product Number: 001
Approval Date: Jul 20, 1992
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information

HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER (HEPARIN SODIUM)
5,000 UNITS/100ML
Marketing Status: Prescription

Active Ingredient: HEPARIN SODIUM
Proprietary Name: HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5,000 UNITS/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019952
Product Number: 004
Approval Date: Jul 20, 1992
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information

HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER (HEPARIN SODIUM)
10,000 UNITS/100ML
Marketing Status: Prescription

Active Ingredient: HEPARIN SODIUM
Proprietary Name: HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10,000 UNITS/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019952
Product Number: 005
Approval Date: Jul 20, 1992
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Prescription
Patent and Exclusivity Information