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FDA NDA · NDA021472

MIDOL LIQUID GELS

Sponsor: BIONPHARMA

APPLICATION
NDA021472
TYPE
NDA
ORIGINAL APPROVAL
2002-10-18
LATEST ACTION
2021-10-21
ROUTE
ORAL
DOSAGE FORM
CAPSULE
MARKETING STATUS
Over-the-counter

Products

MIDOL LIQUID GELS · ReferenceOver-the-counter
IBUPROFEN 200MG · CAPSULE · ORAL

Approval history

2021-10-21Labeling · Supplement 15 · standardLetterAP
2017-03-16Labeling · Supplement 14 · standardLabelAP
2010-04-28Labeling · Supplement 13 · unknownLetterAP
2009-04-15Labeling · Supplement 12 · standardLetterAP
2009-02-19Labeling · Supplement 11 · standardLetterAP
2006-12-18Labeling · Supplement 7 · standardLetterAP
2006-03-13Efficacy · Supplement 5 · standardLabelAP
2005-12-21Labeling · Supplement 6 · standardLetterAP
2004-01-22Labeling · Supplement 1 · standardLabelAP
2002-10-18Type 3 - New Dosage Form · Original · standardReviewAP
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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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