anastrozole

Generic: anastrozole

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-7536
Product ID 0093-7536_a02eea00-78b1-4cf8-93f7-5d43f59722f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078058
Listing Expiration 2026-12-31
Marketing Start 2010-06-28

Pharmacologic Class

Established (EPC)
aromatase inhibitor [epc]
Mechanism of Action
aromatase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00937536
Hyphenated Format 0093-7536

Supplemental Identifiers

RxCUI
199224
UPC
0300937536567
UNII
2Z07MYW1AZ
NUI
N0000175563 N0000175080

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name anastrozole (source: ndc)
Generic Name anastrozole (source: ndc)
Application Number ANDA078058 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (0093-7536-56)
source: ndc

Packages (1)

0093-7536-56 30 TABLET, FILM COATED in 1 BOTTLE (0093-7536-56)

Ingredients (1)

anastrozole (1 mg/1)

Linked Drug Pages (1)

Anastrozole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a02eea00-78b1-4cf8-93f7-5d43f59722f0", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0300937536567"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["c58c7013-50a0-4734-8a78-38ff20a3e7eb"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-7536-56)", "package_ndc": "0093-7536-56", "marketing_start_date": "20100628"}], "brand_name": "Anastrozole", "product_id": "0093-7536_a02eea00-78b1-4cf8-93f7-5d43f59722f0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "0093-7536", "generic_name": "Anastrozole", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anastrozole", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA078058", "marketing_category": "ANDA", "marketing_start_date": "20100628", "listing_expiration_date": "20261231"}