NDC 49884-257 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC49884-257

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Par Health USA, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071839
Marketed since
November 14, 1988
Listing expires
December 31, 2027
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Minoxidil →

Package NDC codes (2)

Package NDCDescriptionSince
49884-257-01100 TABLET in 1 BOTTLE (49884-257-01)Nov 14, 1988
49884-257-05500 TABLET in 1 BOTTLE (49884-257-05)Nov 14, 1988

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