NDC 71839-104 – Fosaprepitant

Fosaprepitant Dimeglumine 150 mg/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC71839-104

Product details

Brand name
Fosaprepitant
Generic name
Fosaprepitant
Labeler
BE Pharmaceuticals Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA212309
Marketed since
October 15, 2019
Listing expires
December 31, 2026
Pharmacologic class
Substance P/Neurokinin-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Fosaprepitant →

Package NDC codes (1)

Package NDCDescriptionSince
71839-104-011 VIAL, SINGLE-DOSE in 1 CARTON (71839-104-01) / 5 mL in 1 VIAL, SINGLE-DOSEOct 15, 2019

Recalls mentioning this NDC

Other Fosaprepitant products