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United States · US · US:16571-659_102210a0-2a43-44c4-aedf-7741b84675ed
Selegiline Hydrochloride
Orange BookUNIISPLATC N04BD01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRising Pharma Holdings, Inc.
CountryUS (United States)
ATC codeN04BD01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11165716590660 CAPSULE in 1 BOTTLE (16571-659-06)
- ndc111657165950500 CAPSULE in 1 BOTTLE (16571-659-50)
Annotations
UNII (FDA Substance ID)
6W731X367Q
SELEGILINE HYDROCHLORIDE
RxCUI 203137
Orange Book
A206803
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": "16571-659_102210a0-2a43-44c4-aedf-7741b84675ed",
"productndc": "16571-659",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "206803",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "Apr 2, 2019"
}
],
"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": "ANDA206803",
"marketing_category": "ANDA",
"nonproprietary_name": "Selegiline Hydrochloride",
"start_marketing_date": "20190402",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code N04BD01.
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