selegiline hydrochloride
Generic: selegiline hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
selegiline hydrochloride
Generic Name
selegiline hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
selegiline hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-2918
Product ID
50090-2918_8fb333d4-21ac-4598-9e18-2a46d718569c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074871
Listing Expiration
2026-12-31
Marketing Start
1997-07-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500902918
Hyphenated Format
50090-2918
Supplemental Identifiers
RxCUI
UNII
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
ANDA074871 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 4 TABLET in 1 BOTTLE (50090-2918-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8fb333d4-21ac-4598-9e18-2a46d718569c", "openfda": {"unii": ["6W731X367Q"], "rxcui": ["859193"], "spl_set_id": ["f286c854-3b8c-44a8-b3b5-c828dbabb207"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE (50090-2918-0)", "package_ndc": "50090-2918-0", "marketing_start_date": "20170314"}], "brand_name": "Selegiline Hydrochloride", "product_id": "50090-2918_8fb333d4-21ac-4598-9e18-2a46d718569c", "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": "50090-2918", "generic_name": "Selegiline Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Selegiline Hydrochloride", "active_ingredients": [{"name": "SELEGILINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA074871", "marketing_category": "ANDA", "marketing_start_date": "19970706", "listing_expiration_date": "20261231"}