FDA NDC Directory · JSON-LD · Markdown

Minoxidil Topical Solution 2%

NDC 51672-2152 · HUMAN OTC DRUG · SOLUTION

Labeler / ManufacturerSUN PHARMACEUTICAL INDUSTRIES, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA218175
Dosage form / routeSOLUTION · TOPICAL
Active ingredientsMINOXIDIL (20 mg/mL)
Marketing started20250901
Package count2

External sources

Source: openFDA. Public-domain (CC0).