NDC 47783-101 – Kalbitor

Ecallantide 10 mg/mL · Injection, Solution · Subcutaneous

Human Prescription Drug 1 recall

Product NDC47783-101

Product details

Brand name
Kalbitor
Generic name
Ecallantide
Labeler
Takeda Pharmaceuticals America, Inc.
Dosage form
Injection, Solution
Route
Subcutaneous
Marketing category
BLA · BLA125277
Marketed since
February 2, 2010
Listing expires
December 31, 2026
Pharmacologic class
Plasma Kallikrein Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Kalbitor →

Package NDC codes (1)

Package NDCDescriptionSince
47783-101-013 VIAL, GLASS in 1 CARTON (47783-101-01) / 1 mL in 1 VIAL, GLASSFeb 2, 2010

Recalls mentioning this NDC