NDC 42291-618 – Minoxidil

Minoxidil 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC42291-618

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
AvKARE
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072708
Marketed since
August 1, 2013
Listing expires
December 31, 2027
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Minoxidil →

Package NDC codes (1)

Package NDCDescriptionSince
42291-618-01100 TABLET in 1 BOTTLE (42291-618-01)Aug 1, 2013

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