Package 62135-694-60

Brand: selegiline hydrochloride

Generic: selegiline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-694-60
Digits Only 6213569460
Product NDC 62135-694
Description

60 TABLET in 1 BOTTLE (62135-694-60)

Marketing

Marketing Status
Marketed Since 2024-05-06
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": "17f2fc17-a150-214b-e063-6294a90ab548", "openfda": {"upc": ["0362135694609"], "unii": ["6W731X367Q"], "rxcui": ["859193"], "spl_set_id": ["189ac32d-28b4-47c5-9de6-318e502eff3b"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (62135-694-60)", "package_ndc": "62135-694-60", "marketing_start_date": "20240506"}], "brand_name": "Selegiline Hydrochloride", "product_id": "62135-694_17f2fc17-a150-214b-e063-6294a90ab548", "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": "62135-694", "generic_name": "Selegiline Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Selegiline Hydrochloride", "active_ingredients": [{"name": "SELEGILINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA074565", "marketing_category": "ANDA", "marketing_start_date": "19960802", "listing_expiration_date": "20261231"}