NDC 24208-539 – Miochol E

· Kit

Human Prescription Drug 1 recall

Product NDC24208-539

Product details

Brand name
Miochol E
Generic name
Acetylcholine chloride
Labeler
Bausch & Lomb Incorporated
Dosage form
Kit
Marketing category
NDA · NDA020213
Marketed since
September 22, 1993
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Miochol E →

    Package NDC codes (1)

    Package NDCDescriptionSince
    24208-539-201 KIT in 1 BLISTER PACK (24208-539-20) * 2 mL in 1 VIAL * 2 mL in 1 AMPULESep 22, 1993

    Recalls mentioning this NDC