Package 73141-006-02
Brand: selegiline hydrochloride
Generic: selegiline hydrochloridePackage Facts
Identity
Package NDC
73141-006-02
Digits Only
7314100602
Product NDC
73141-006
Description
60 TABLET in 1 BOTTLE (73141-006-02)
Marketing
Marketing Status
Brand
selegiline hydrochloride
Generic
selegiline hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "339f9a9e-dffc-daac-e063-6294a90ae1fe", "openfda": {"upc": ["0373141006027"], "unii": ["6W731X367Q"], "rxcui": ["859193"], "spl_set_id": ["a59ff47b-4379-44f3-9d2c-f8c6121d1881"], "manufacturer_name": ["A2A Integrated Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (73141-006-02)", "package_ndc": "73141-006-02", "marketing_start_date": "20240315"}], "brand_name": "Selegiline Hydrochloride", "product_id": "73141-006_339f9a9e-dffc-daac-e063-6294a90ae1fe", "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": "73141-006", "generic_name": "Selegiline Hydrochloride", "labeler_name": "A2A Integrated Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Selegiline Hydrochloride", "active_ingredients": [{"name": "SELEGILINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA074672", "marketing_category": "ANDA", "marketing_start_date": "20240315", "listing_expiration_date": "20261231"}