Package 50090-2918-0

Brand: selegiline hydrochloride

Generic: selegiline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-2918-0
Digits Only 5009029180
Product NDC 50090-2918
Product ID 50090-2918_8fb333d4-21ac-4598-9e18-2a46d718569c
Description

4 TABLET in 1 BOTTLE (50090-2918-0)

Marketing

Marketing Status
Marketed Since 2017-03-14
Brand selegiline hydrochloride
Generic selegiline hydrochloride
Sample Package No

Linked Drug Pages (1)

Selegiline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8fb333d4-21ac-4598-9e18-2a46d718569c", "openfda": {"unii": ["6W731X367Q"], "rxcui": ["859193"], "spl_set_id": ["f286c854-3b8c-44a8-b3b5-c828dbabb207"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE (50090-2918-0)", "package_ndc": "50090-2918-0", "marketing_start_date": "20170314"}], "brand_name": "Selegiline Hydrochloride", "product_id": "50090-2918_8fb333d4-21ac-4598-9e18-2a46d718569c", "dosage_form": "TABLET", "pharm_class": ["Monoamine Oxidase Inhibitor [EPC]", "Monoamine Oxidase Inhibitors [MoA]", "Monoamine Oxidase Type B Inhibitor [EPC]", "Monoamine Oxidase-B Inhibitors [MoA]"], "product_ndc": "50090-2918", "generic_name": "Selegiline Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Selegiline Hydrochloride", "active_ingredients": [{"name": "SELEGILINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA074871", "marketing_category": "ANDA", "marketing_start_date": "19970706", "listing_expiration_date": "20261231"}