NDC 0093-3133 – Imiquimod

Imiquimod 37.5 mg/g · Cream · Topical

Human Prescription Drug

Product NDC0093-3133

Product details

Brand name
Imiquimod
Generic name
Imiquimod
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Cream
Route
Topical
Marketing category
NDA AUTHORIZED GENERIC · NDA022483
Marketed since
July 30, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Imiquimod →

Package NDC codes (1)

Package NDCDescriptionSince
0093-3133-311 BOTTLE, PUMP in 1 CARTON (0093-3133-31) / 7.5 g in 1 BOTTLE, PUMPJul 30, 2020

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