NDC directory

MINOXIDIL (FOR MEN)

Minoxidil · FlexiGo Inc · AEROSOL, FOAM

85524-2612ANDAArteriolar Vasodilation [PE]
Product NDC
85524-2612
Generic name
Minoxidil
Labeler name
FlexiGo Inc
Brand name
MINOXIDIL (FOR MEN)
Finished
true
Listing expiration date
20271231
Marketing category
ANDA
Dosage form
AEROSOL, FOAM
SPL ID
5f574daf-7879-ae49-e063-6394a90ae0d0
Product type
HUMAN OTC DRUG
Marketing start date
20261102
Product ID
85524-2612_5f574daf-7879-ae49-e063-6394a90ae0d0
Application number
ANDA218616
Brand name base
MINOXIDIL (FOR MEN)
Active ingredients
  1. Name
    MINOXIDIL
    Strength
    5 g/100g
Packaging
  1. Package NDC
    85524-2612-2
    Description
    1 BOTTLE in 1 BOX (85524-2612-2) / 60 g in 1 BOTTLE (85524-2612-1)
    Marketing start date
    20261102
    Sample
    false
Route
TOPICAL
Pharm class
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.