NDC 55513-132 – Kanjinti

Trastuzumab 420 mg/20mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC55513-132

Product details

Brand name
Kanjinti
Generic name
Trastuzumab-anns
Labeler
Amgen, Inc
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
BLA · BLA761073
Marketed since
June 11, 2019
Listing expires
December 31, 2027
Pharmacologic class
HER2/neu Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Kanjinti →

Package NDC codes (2)

Package NDCDescriptionSince
55513-132-011 VIAL, MULTI-DOSE in 1 CARTON (55513-132-01) / 20 mL in 1 VIAL, MULTI-DOSEJun 11, 2019
55513-132-211 VIAL, MULTI-DOSE in 1 CARTON (55513-132-21) / 20 mL in 1 VIAL, MULTI-DOSEJul 1, 2025

Other Kanjinti products