NDC 68001-155 – Anastrozole

Anastrozole 1 mg/1 · Tablet, Coated · Oral

Human Prescription Drug 1 recall

Product NDC68001-155

Product details

Brand name
Anastrozole
Generic name
Anastrozole
Labeler
BluePoint Laboratories
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA078921
Marketed since
January 1, 2014
Listing expires
December 31, 2026
Pharmacologic class
Aromatase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Anastrozole →

Package NDC codes (2)

Package NDCDescriptionSince
68001-155-0430 TABLET, COATED in 1 BOTTLE (68001-155-04)Jan 1, 2014
68001-155-081000 TABLET, COATED in 1 BOTTLE (68001-155-08)Jan 1, 2014

Recalls mentioning this NDC

Other Anastrozole products