NDC 47335-361 – Decitabine

· Kit

Human Prescription Drug 1 recall

Product NDC47335-361

Product details

Brand name
Decitabine
Generic name
Decitabine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Kit
Marketing category
NDA · NDA205582
Marketed since
January 24, 2014
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Decitabine →

    Package NDC codes (1)

    Package NDCDescriptionSince
    47335-361-411 KIT in 1 CARTON (47335-361-41) * 10 mL in 1 VIAL, SINGLE-DOSE * 10 mL in 1 VIAL (47335-362-40)Jan 24, 2014

    Recalls mentioning this NDC

    Other Decitabine products