NDC 0310-3200 – Andexxa

Andexanet Alfa 200 mg/20mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC0310-3200

Product details

Brand name
Andexxa
Generic name
Andexanet alfa
Labeler
AstraZeneca Pharmaceuticals LP
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
BLA · BLA125586
Marketed since
July 12, 2022
Marketing end
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Andexxa →

Package NDC codes (2)

Package NDCDescriptionSince
0310-3200-044 VIAL, SINGLE-USE in 1 CARTON (0310-3200-04) / 20 mL in 1 VIAL, SINGLE-USE (0310-3200-01)Jul 12, 2022
0310-3200-055 VIAL, SINGLE-USE in 1 CARTON (0310-3200-05) / 20 mL in 1 VIAL, SINGLE-USE (0310-3200-01)Jul 3, 2023