NDC 68382-209 – Anastrozole

Anastrozole 1 mg/1 · Tablet, Coated · Oral

Human Prescription Drug 2 recalls

Product NDC68382-209

Product details

Brand name
Anastrozole
Generic name
Anastrozole
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA078921
Marketed since
June 27, 2010
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
68382-209-0630 TABLET, COATED in 1 BOTTLE (68382-209-06)Jun 27, 2010
68382-209-101000 TABLET, COATED in 1 BOTTLE (68382-209-10)Jun 27, 2010

Recalls mentioning this NDC

Other Anastrozole products