anastrozole

Generic: anastrozole

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

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3853
Product ID 68071-3853_4587a0ae-889c-26c8-e063-6394a90adb3f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079220
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 680713853
Hyphenated Format 68071-3853

Supplemental Identifiers

RxCUI
199224
UPC
0368071385380
UNII
2Z07MYW1AZ
NUI
N0000175563 N0000175080

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 ANDA079220 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 12 TABLET in 1 BOTTLE (68071-3853-7)
  • 8 TABLET in 1 BOTTLE (68071-3853-8)
source: ndc

Packages (2)

68071-3853-7 12 TABLET in 1 BOTTLE (68071-3853-7) 68071-3853-8 8 TABLET in 1 BOTTLE (68071-3853-8)

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": "4587a0ae-889c-26c8-e063-6394a90adb3f", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0368071385380"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["362034e9-2830-19a5-e063-6394a90a8dfb"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (68071-3853-7)", "package_ndc": "68071-3853-7", "marketing_start_date": "20251209"}, {"sample": false, "description": "8 TABLET in 1 BOTTLE (68071-3853-8)", "package_ndc": "68071-3853-8", "marketing_start_date": "20250527"}], "brand_name": "ANASTROZOLE", "product_id": "68071-3853_4587a0ae-889c-26c8-e063-6394a90adb3f", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "68071-3853", "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": "ANDA079220", "marketing_category": "ANDA", "marketing_start_date": "20100628", "listing_expiration_date": "20261231"}