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United States · US · US:70954-504_e42d99b0-c62e-49d4-b792-1301bb539b92
Selegiline Hydrochloride
Orange BookUNIISPLATC N04BD01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNovitium Pharma LLC
CountryUS (United States)
ATC codeN04BD01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11709545041060 CAPSULE in 1 BOTTLE (70954-504-10)
- ndc1170954504201000 CAPSULE in 1 BOTTLE (70954-504-20)
Annotations
UNII (FDA Substance ID)
6W731X367Q
SELEGILINE HYDROCHLORIDE
RxCUI 203137
Orange Book
A075352
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": "70954-504_e42d99b0-c62e-49d4-b792-1301bb539b92",
"productndc": "70954-504",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "075352",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "Nov 30, 1998"
}
],
"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": "ANDA075352",
"marketing_category": "ANDA",
"nonproprietary_name": "Selegiline Hydrochloride",
"start_marketing_date": "20210401",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code N04BD01.
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