anastrozole

Generic: anastrozole tablets

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole tablets
Labeler upsher-smith laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-725
Product ID 24979-725_398a1cb9-25cd-a30d-e063-6394a90a1956
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206037
Listing Expiration 2026-12-31
Marketing Start 2025-03-21

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 24979725
Hyphenated Format 24979-725

Supplemental Identifiers

RxCUI
199224
UPC
0324979725079
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 tablets (source: ndc)
Application Number ANDA206037 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (24979-725-06)
  • 90 TABLET in 1 BOTTLE (24979-725-07)
source: ndc

Packages (2)

Ingredients (1)

anastrozole (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "398a1cb9-25cd-a30d-e063-6394a90a1956", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0324979725079"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["7e0bd2cc-d3cc-403f-a6b6-4597ccb2f685"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (24979-725-06)", "package_ndc": "24979-725-06", "marketing_start_date": "20250321"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (24979-725-07)", "package_ndc": "24979-725-07", "marketing_start_date": "20250321"}], "brand_name": "Anastrozole", "product_id": "24979-725_398a1cb9-25cd-a30d-e063-6394a90a1956", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "24979-725", "generic_name": "Anastrozole Tablets", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anastrozole", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA206037", "marketing_category": "ANDA", "marketing_start_date": "20250321", "listing_expiration_date": "20261231"}