NDC 71335-3145 – Anastrozole

Anastrozole 1 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-3145

Product details

Brand name
Anastrozole
Generic name
Anastrozole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA078921
Marketed since
June 27, 2010
Listing expires
December 31, 2027
Pharmacologic class
Aromatase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Anastrozole →

Package NDC codes (10)

Package NDCDescriptionSince
71335-3145-028 TABLET, COATED in 1 BOTTLE (71335-3145-0)Jun 18, 2026
71335-3145-130 TABLET, COATED in 1 BOTTLE (71335-3145-1)Jun 18, 2026
71335-3145-220 TABLET, COATED in 1 BOTTLE (71335-3145-2)Jun 18, 2026
71335-3145-390 TABLET, COATED in 1 BOTTLE (71335-3145-3)Jun 18, 2026
71335-3145-44 TABLET, COATED in 1 BOTTLE (71335-3145-4)Jun 18, 2026
71335-3145-56 TABLET, COATED in 1 BOTTLE (71335-3145-5)Jun 18, 2026
71335-3145-610 TABLET, COATED in 1 BOTTLE (71335-3145-6)Jun 18, 2026
71335-3145-740 TABLET, COATED in 1 BOTTLE (71335-3145-7)Jun 18, 2026
71335-3145-812 TABLET, COATED in 1 BOTTLE (71335-3145-8)Jun 18, 2026
71335-3145-914 TABLET, COATED in 1 BOTTLE (71335-3145-9)Jun 18, 2026

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