Package 80005-116-02

Brand: lomustine

Generic: lomustine
NDC Package

Package Facts

Identity

Package NDC 80005-116-02
Digits Only 8000511602
Product NDC 80005-116
Description

5 CAPSULE in 1 BOTTLE (80005-116-02)

Marketing

Marketing Status
Marketed Since 2025-11-10
Brand lomustine
Generic lomustine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42672c94-b4e6-4bb8-b6b4-7c429acd7ea2", "openfda": {"nui": ["N0000000236", "N0000175558"], "upc": ["0380005116020"], "unii": ["7BRF0Z81KG"], "rxcui": ["197894", "197895", "197896"], "spl_set_id": ["916dfac8-da11-40e4-9e44-a909e29a6b5f"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Carnegie Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 CAPSULE in 1 BOTTLE (80005-116-02)", "package_ndc": "80005-116-02", "marketing_start_date": "20251110"}], "brand_name": "LOMUSTINE", "product_id": "80005-116_42672c94-b4e6-4bb8-b6b4-7c429acd7ea2", "dosage_form": "CAPSULE", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "80005-116", "generic_name": "LOMUSTINE", "labeler_name": "Carnegie Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOMUSTINE", "active_ingredients": [{"name": "LOMUSTINE", "strength": "100 mg/1"}], "application_number": "ANDA219265", "marketing_category": "ANDA", "marketing_start_date": "20251110", "listing_expiration_date": "20261231"}