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FDA ANDA · ANDA207449

DEXTROSE

dextrose monohydrate

Sponsor: FRESENIUS KABI USA

APPLICATION
ANDA207449
TYPE
ANDA
ORIGINAL APPROVAL
2016-10-21
LATEST ACTION
2026-07-14
ROUTE
INTRAVENOUS, INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Prescription

Products

DEXTROSE 5% IN PLASTIC CONTAINERPrescription
DEXTROSE 50MG/ML · INJECTABLE · INJECTION

Approval history

2026-07-14Labeling · Supplement 30 · standardAP
2022-07-20Manufacturing (CMC) · Supplement 19 · unknownAP
2020-11-20Manufacturing (CMC) · Supplement 14 · unknownAP
2018-06-26Labeling · Supplement 3 · standardAP
2016-10-21UNKNOWN · Original · standardLetterAP
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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