NDC 0093-7536 – Anastrozole

Anastrozole 1 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0093-7536

Product details

Brand name
Anastrozole
Generic name
Anastrozole
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078058
Marketed since
June 28, 2010
Listing expires
December 31, 2026
Pharmacologic class
Aromatase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Anastrozole →

Package NDC codes (1)

Package NDCDescriptionSince
0093-7536-5630 TABLET, FILM COATED in 1 BOTTLE (0093-7536-56)Jun 28, 2010

Other Anastrozole products