NDC 70710-1688 – Fulvestrant

Fulvestrant 50 mg/mL · Injection, Solution · Intramuscular

Human Prescription Drug 1 recall

Product NDC70710-1688

Product details

Brand name
Fulvestrant
Generic name
Fulvestrant
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Injection, Solution
Route
Intramuscular
Marketing category
ANDA · ANDA215234
Marketed since
December 14, 2021
Listing expires
December 31, 2026
Pharmacologic class
Estrogen Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Fulvestrant →

Package NDC codes (1)

Package NDCDescriptionSince
70710-1688-82 SYRINGE, GLASS in 1 CARTON (70710-1688-8) / 5 mL in 1 SYRINGE, GLASS (70710-1688-2)Dec 14, 2021

Recalls mentioning this NDC

Other Fulvestrant products