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FDA ANDA · ANDA078998

IBANDRONATE SODIUM

Sponsor: ORBION PHARMS

APPLICATION
ANDA078998
TYPE
ANDA
ORIGINAL APPROVAL
2012-03-19
LATEST ACTION
2026-02-03
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription

Products

IBANDRONATE SODIUMPrescription
IBANDRONATE SODIUM EQ 150MG BASE · TABLET · ORAL

Approval history

2026-02-03Labeling · Supplement 8 · standardAP
2023-02-15Labeling · Supplement 4 · standardAP
2015-07-15Labeling · Supplement 2 · standardAP
2015-07-15Labeling · Supplement 3 · standardAP
2012-03-19OriginalReviewAP
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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