selegiline hydrochloride
Generic: selegiline hydrochloride
Labeler: apotex corp.Drug Facts
Product Profile
Brand Name
selegiline hydrochloride
Generic Name
selegiline hydrochloride
Labeler
apotex corp.
Dosage Form
CAPSULE
Routes
Active Ingredients
selegiline hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60505-0055
Product ID
60505-0055_2a0cd745-7f62-19e1-d623-fea131789df0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075321
Listing Expiration
2026-12-31
Marketing Start
1997-07-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605050055
Hyphenated Format
60505-0055
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
selegiline hydrochloride (source: ndc)
Generic Name
selegiline hydrochloride (source: ndc)
Application Number
ANDA075321 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 60 CAPSULE in 1 BOTTLE (60505-0055-1)
- 1000 CAPSULE in 1 BOTTLE (60505-0055-2)
- 500 CAPSULE in 1 BOTTLE (60505-0055-3)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a0cd745-7f62-19e1-d623-fea131789df0", "openfda": {"unii": ["6W731X367Q"], "rxcui": ["859186"], "spl_set_id": ["1924db3d-6a16-4496-cfd0-6903be146925"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (60505-0055-1)", "package_ndc": "60505-0055-1", "marketing_start_date": "19970715"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (60505-0055-2)", "package_ndc": "60505-0055-2", "marketing_start_date": "19970715"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (60505-0055-3)", "package_ndc": "60505-0055-3", "marketing_start_date": "19970715"}], "brand_name": "SELEGILINE HYDROCHLORIDE", "product_id": "60505-0055_2a0cd745-7f62-19e1-d623-fea131789df0", "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": "60505-0055", "generic_name": "SELEGILINE HYDROCHLORIDE", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SELEGILINE HYDROCHLORIDE", "active_ingredients": [{"name": "SELEGILINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA075321", "marketing_category": "ANDA", "marketing_start_date": "19970715", "listing_expiration_date": "20261231"}