anastrozole

Generic: anastrozole

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole
Labeler american health packaging
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-112
Product ID 60687-112_3d83a46b-4eef-64dc-e063-6294a90aa390
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078921
Listing Expiration 2026-12-31
Marketing Start 2016-02-03

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 60687112
Hyphenated Format 60687-112

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 ANDA078921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-112-21) / 1 TABLET, COATED in 1 BLISTER PACK (60687-112-11)
source: ndc

Packages (1)

Ingredients (1)

anastrozole (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d83a46b-4eef-64dc-e063-6294a90aa390", "openfda": {"nui": ["N0000175563", "N0000175080"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["dface914-5135-4136-82f4-75429b496a35"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-112-21)  / 1 TABLET, COATED in 1 BLISTER PACK (60687-112-11)", "package_ndc": "60687-112-21", "marketing_start_date": "20160203"}], "brand_name": "Anastrozole", "product_id": "60687-112_3d83a46b-4eef-64dc-e063-6294a90aa390", "dosage_form": "TABLET, COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "60687-112", "generic_name": "Anastrozole", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anastrozole", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA078921", "marketing_category": "ANDA", "marketing_start_date": "20160203", "listing_expiration_date": "20261231"}