NDC 72789-279 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-279

Product details

Brand name
Minoxidil
Generic name
minoxidil
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072709
Marketed since
December 14, 1995
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
72789-279-01100 TABLET in 1 BOTTLE, PLASTIC (72789-279-01)Oct 7, 2022

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