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United States · US · US:50090-2918_8fb333d4-21ac-4598-9e18-2a46d718569c

Selegiline Hydrochloride

Orange BookUNIISPLATC N04BD01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeN04BD01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5009029180
    4 TABLET in 1 BOTTLE (50090-2918-0)

Annotations

UNII (FDA Substance ID)
6W731X367Q
SELEGILINE HYDROCHLORIDE
RxCUI 203137
Orange Book
A074871
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "6W731X367Q",
    "rxcui": "203137",
    "inchikey": "IYETZZCWLLUHIJ-UTONKHPSSA-N",
    "display_name": "SELEGILINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "040a97e5-efd1-4a2f-b737-2f13e5366d70": {
      "match": "brand_token",
      "title": "SELEGILINE HYDROCHLORIDE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]",
      "spl_version": "10",
      "published_date": "2025-12-08"
    }
  },
  "productid": "50090-2918_8fb333d4-21ac-4598-9e18-2a46d718569c",
  "productndc": "50090-2918",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "074871",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Jun 6, 1997"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SELEGILINE HYDROCHLORIDE",
  "proprietary_name": "Selegiline Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA074871",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Selegiline Hydrochloride",
  "start_marketing_date": "19970706",
  "active_numerator_strength": "5"
}

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