Package 71335-2673-1

Brand: selegiline hydrochloride

Generic: selegiline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2673-1
Digits Only 7133526731
Product NDC 71335-2673
Description

30 CAPSULE in 1 BOTTLE (71335-2673-1)

Marketing

Marketing Status
Marketed Since 2025-07-15
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": "f2fc35e0-f99a-4a92-85d4-1e2d1f9fbac2", "openfda": {"unii": ["6W731X367Q"], "rxcui": ["859186"], "spl_set_id": ["4848270a-1179-410c-b4e6-a7e555b3a988"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-2673-1)", "package_ndc": "71335-2673-1", "marketing_start_date": "20250715"}], "brand_name": "Selegiline Hydrochloride", "product_id": "71335-2673_f2fc35e0-f99a-4a92-85d4-1e2d1f9fbac2", "dosage_form": "CAPSULE", "pharm_class": ["Monoamine Oxidase Inhibitor [EPC]", "Monoamine Oxidase Inhibitors [MoA]", "Monoamine Oxidase Type B Inhibitor [EPC]", "Monoamine Oxidase-B Inhibitors [MoA]"], "product_ndc": "71335-2673", "generic_name": "Selegiline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Selegiline Hydrochloride", "active_ingredients": [{"name": "SELEGILINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA206803", "marketing_category": "ANDA", "marketing_start_date": "20190402", "listing_expiration_date": "20261231"}