NDC 0574-0621 – Podofilox

Podofilox 5 mg/g · Gel · Topical

Human Prescription Drug

Product NDC0574-0621

Product details

Brand name
Podofilox
Generic name
Podofilox
Labeler
Padagis US LLC
Dosage form
Gel
Route
Topical
Marketing category
ANDA · ANDA211871
Marketed since
December 13, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Podofilox →

Package NDC codes (1)

Package NDCDescriptionSince
0574-0621-053.5 g in 1 TUBE, WITH APPLICATOR (0574-0621-05)Dec 13, 2023

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