Package 0093-7536-56
Brand: anastrozole
Generic: anastrozolePackage Facts
Identity
Package NDC
0093-7536-56
Digits Only
0093753656
Product NDC
0093-7536
Description
30 TABLET, FILM COATED in 1 BOTTLE (0093-7536-56)
Marketing
Marketing Status
Brand
anastrozole
Generic
anastrozole
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a02eea00-78b1-4cf8-93f7-5d43f59722f0", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0300937536567"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["c58c7013-50a0-4734-8a78-38ff20a3e7eb"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-7536-56)", "package_ndc": "0093-7536-56", "marketing_start_date": "20100628"}], "brand_name": "Anastrozole", "product_id": "0093-7536_a02eea00-78b1-4cf8-93f7-5d43f59722f0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "0093-7536", "generic_name": "Anastrozole", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anastrozole", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA078058", "marketing_category": "ANDA", "marketing_start_date": "20100628", "listing_expiration_date": "20261231"}