NDC 0591-5642 – Minoxidil

Minoxidil 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0591-5642

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071344
Marketed since
October 26, 2009
Listing expires
December 31, 2026
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Minoxidil →

Package NDC codes (2)

Package NDCDescriptionSince
0591-5642-01100 TABLET in 1 BOTTLE, PLASTIC (0591-5642-01)Oct 26, 2009
0591-5642-05500 TABLET in 1 BOTTLE, PLASTIC (0591-5642-05)Oct 26, 2009

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