anastrozole

Generic: anastrozole

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5002
Product ID 50090-5002_3ad4f75a-24ea-45dc-96f3-18f49865a38f
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 500905002
Hyphenated Format 50090-5002

Supplemental Identifiers

RxCUI
199224
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
  • 30 TABLET in 1 BOTTLE (50090-5002-0)
  • 90 TABLET in 1 BOTTLE (50090-5002-1)
source: ndc

Packages (2)

50090-5002-0 30 TABLET in 1 BOTTLE (50090-5002-0) 50090-5002-1 90 TABLET in 1 BOTTLE (50090-5002-1)

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": "3ad4f75a-24ea-45dc-96f3-18f49865a38f", "openfda": {"nui": ["N0000175563", "N0000175080"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["90d9dbb4-b1ba-431e-b588-1a1a04cf1444"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5002-0)", "package_ndc": "50090-5002-0", "marketing_start_date": "20200409"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5002-1)", "package_ndc": "50090-5002-1", "marketing_start_date": "20200409"}], "brand_name": "ANASTROZOLE", "product_id": "50090-5002_3ad4f75a-24ea-45dc-96f3-18f49865a38f", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "50090-5002", "generic_name": "ANASTROZOLE", "labeler_name": "A-S Medication Solutions", "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"}