NDCFind

Minoxidil 53489-0386-03

Package NDC

53489-0386-03

Product NDC: 53489-0386

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
December 14, 1995
Listing Expires
December 31, 2027
Application
ANDA072709
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Active Ingredients

IngredientStrength
Minoxidil2.5 mg/1

Drug Class

Arteriolar Vasodilator [EPC]Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]

Selected Package

53489-0386-03Selected

250 TABLET in 1 BOTTLE (53489-386-03)

Other packages for this product(3)

100 TABLET in 1 BOTTLE (53489-386-01)

500 TABLET in 1 BOTTLE (53489-386-05)

1000 TABLET in 1 BOTTLE (53489-386-10)