NDC 68462-317 – Fulvestrant

Fulvestrant 50 mg/mL · Injection · Intramuscular

Human Prescription Drug 1 recall

Product NDC68462-317

Product details

Brand name
Fulvestrant
Generic name
Fulvestrant
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Dosage form
Injection
Route
Intramuscular
Marketing category
ANDA · ANDA207754
Marketed since
August 22, 2019
Listing expires
December 31, 2027
Pharmacologic class
Estrogen Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Fulvestrant →

Package NDC codes (1)

Package NDCDescriptionSince
68462-317-322 SYRINGE, GLASS in 1 CARTON (68462-317-32) / 5 mL in 1 SYRINGE, GLASS (68462-317-40)Aug 22, 2019

Recalls mentioning this NDC

Other Fulvestrant products