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FDA ANDA · ANDA203851

HEPARIN SODIUM

Sponsor: PHARMOBEDIENT

APPLICATION
ANDA203851
TYPE
ANDA
ORIGINAL APPROVAL
2017-11-30
LATEST ACTION
2020-07-29
ROUTE
INTRAVENOUS, SUBCUTANEOUS, INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Prescription

Products

HEPARIN SODIUMPrescription
HEPARIN SODIUM 5,000 UNITS/ML · INJECTABLE · INJECTION
HEPARIN SODIUMPrescription
HEPARIN SODIUM 10,000 UNITS/ML · INJECTABLE · INJECTION
HEPARIN SODIUMPrescription
HEPARIN SODIUM 1,000 UNITS/ML · INJECTABLE · INJECTION

Approval history

2020-07-29Labeling · Supplement 10 · standardAP
2017-11-30UNKNOWN · OriginalLetterAP
VIEW ON DRUGS@FDA ↗

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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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