Heparin group

Heparin Sodium 25,000 Units in Sodium Chloride 0.45% in Plastic Container

Approved 20 Jul 1992InjectionInjectable

The FDA lists this product in 6 strengths and forms.

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Composition

Active ingredients: HEPARIN SODIUM 5,000 UNITS/100ML

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

HEPARIN SODIUM 10,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA019802-002 · Discontinued
HEPARIN SODIUM 5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA019802-005 · Discontinued
HEPARIN SODIUM 10,000 UNITS/100ML · InjectableNDA019953-004 · Prescription
HEPARIN SODIUM 5,000 UNITS/100ML · InjectableThis page
HEPARIN SODIUM 5,000 UNITS/100ML · InjectableNDA018916-007 · Prescription
HEPARIN SODIUM 10,000 UNITS/100ML · Injectable

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NDA018916-008 · Prescription

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application NDA019953.

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Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Brand name: Heparin Sodium 25,000 Units in Sodium Chloride 0.45% in Plastic Container
Active substance: heparin sodium
Drug class: Heparin group, Heparins or heparinoids for topical use, Other ophthalmologicals
Group: Anticoagulants and antiplatelets
Route: Injection
Dosage form: Injectable
Applicant: B Braun
Status: Prescription
FDA approval: 20 Jul 1992
Application: NDA019953-003
RxCUI: 314659