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United States · US · US:72319-006_248576e6-bc11-e847-e063-6294a90afe9d

Selegiline Hydrochloride

Orange BookUNIISPLATC N04BD01

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

Identification

Manufactureri3 Pharmaceuticals, LLC
CountryUS (United States)
ATC codeN04BD01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7231900602
    60 TABLET in 1 BOTTLE (72319-006-02)

Annotations

UNII (FDA Substance ID)
6W731X367Q
SELEGILINE HYDROCHLORIDE
RxCUI 203137
Orange Book
A074672
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": "72319-006_248576e6-bc11-e847-e063-6294a90afe9d",
  "productndc": "72319-006",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "074672",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Apr 1, 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": "ANDA074672",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Selegiline Hydrochloride",
  "start_marketing_date": "20211215",
  "active_numerator_strength": "5"
}

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