selegiline hydrochloride

Generic: selegiline hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name selegiline hydrochloride
Generic Name selegiline hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

selegiline hydrochloride 5 mg/1

Manufacturer
A-S Medication Solutions

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
monoamine oxidase inhibitor [epc] monoamine oxidase inhibitors [moa] monoamine oxidase type b inhibitor [epc] monoamine oxidase-b inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902918
Hyphenated Format 50090-2918

Supplemental Identifiers

RxCUI
859193
UNII
6W731X367Q

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 4 TABLET in 1 BOTTLE (50090-2918-0)
source: ndc

Packages (1)

Ingredients (1)

selegiline hydrochloride (5 mg/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"}