Package 72319-006-02
Brand: selegiline hydrochloride
Generic: selegiline hydrochloridePackage Facts
Identity
Package NDC
72319-006-02
Digits Only
7231900602
Product NDC
72319-006
Description
60 TABLET in 1 BOTTLE (72319-006-02)
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": "248576e6-bc11-e847-e063-6294a90afe9d", "openfda": {"upc": ["0372319006029"], "unii": ["6W731X367Q"], "rxcui": ["859193"], "spl_set_id": ["c81e983b-455d-2e65-e053-2a95a90a3123"], "manufacturer_name": ["i3 Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72319-006-02)", "package_ndc": "72319-006-02", "marketing_start_date": "20211215"}], "brand_name": "Selegiline Hydrochloride", "product_id": "72319-006_248576e6-bc11-e847-e063-6294a90afe9d", "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": "72319-006", "generic_name": "Selegiline Hydrochloride", "labeler_name": "i3 Pharmaceuticals, LLC", "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": "20211215", "listing_expiration_date": "20261231"}