anastrozole
Generic: anastrozole
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
anastrozole
Generic Name
anastrozole
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
anastrozole 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-2791
Product ID
68071-2791_31e27616-7902-a78b-e063-6394a90a5f5a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090568
Listing Expiration
2026-12-31
Marketing Start
2010-06-22
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680712791
Hyphenated Format
68071-2791
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA090568 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 8 TABLET in 1 BOTTLE, PLASTIC (68071-2791-0)
- 20 TABLET in 1 BOTTLE, PLASTIC (68071-2791-2)
- 15 TABLET in 1 BOTTLE, PLASTIC (68071-2791-5)
- 12 TABLET in 1 BOTTLE, PLASTIC (68071-2791-7)
- 180 TABLET in 1 BOTTLE, PLASTIC (68071-2791-8)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31e27616-7902-a78b-e063-6394a90a5f5a", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0368071279153"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["e3b5fc92-9189-6944-e053-2a95a90a1c9f"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET in 1 BOTTLE, PLASTIC (68071-2791-0)", "package_ndc": "68071-2791-0", "marketing_start_date": "20250317"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (68071-2791-2)", "package_ndc": "68071-2791-2", "marketing_start_date": "20220713"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (68071-2791-5)", "package_ndc": "68071-2791-5", "marketing_start_date": "20220713"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (68071-2791-7)", "package_ndc": "68071-2791-7", "marketing_start_date": "20250103"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (68071-2791-8)", "package_ndc": "68071-2791-8", "marketing_start_date": "20220713"}], "brand_name": "Anastrozole", "product_id": "68071-2791_31e27616-7902-a78b-e063-6394a90a5f5a", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "68071-2791", "generic_name": "Anastrozole", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anastrozole", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA090568", "marketing_category": "ANDA", "marketing_start_date": "20100622", "listing_expiration_date": "20261231"}