anastrozole

Generic: anastrozole

Labeler: breckenridge pharmaceutical, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole
Labeler breckenridge pharmaceutical, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
Breckenridge Pharmaceutical, Inc.

Identifiers & Regulatory

Product NDC 51991-620
Product ID 51991-620_d127732f-9c07-4d93-b8df-fd4019cb31e0
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 51991620
Hyphenated Format 51991-620

Supplemental Identifiers

RxCUI
199224
UPC
0351991620907
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 ANDA079220 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (51991-620-10)
  • 30 TABLET in 1 BOTTLE (51991-620-33)
  • 90 TABLET in 1 BOTTLE (51991-620-90)
source: ndc

Packages (3)

51991-620-10 1000 TABLET in 1 BOTTLE (51991-620-10) 51991-620-33 30 TABLET in 1 BOTTLE (51991-620-33) 51991-620-90 90 TABLET in 1 BOTTLE (51991-620-90)

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": "d127732f-9c07-4d93-b8df-fd4019cb31e0", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0351991620907"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["ca9d4aff-ffdf-4a46-ad20-e47e5886a19e"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (51991-620-10)", "package_ndc": "51991-620-10", "marketing_start_date": "20100628"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (51991-620-33)", "package_ndc": "51991-620-33", "marketing_start_date": "20100628"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (51991-620-90)", "package_ndc": "51991-620-90", "marketing_start_date": "20230401"}], "brand_name": "ANASTROZOLE", "product_id": "51991-620_d127732f-9c07-4d93-b8df-fd4019cb31e0", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "51991-620", "generic_name": "ANASTROZOLE", "labeler_name": "Breckenridge Pharmaceutical, 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"}