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United States · US · US:59762-0119_d7302106-710a-49a4-9ab4-2de28937306c
phenelzine sulfate
Orange BookUNIISPLATC N06AF
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMylan Pharmaceuticals Inc.
CountryUS (United States)
ATC codeN06AF
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11597620119160 TABLET, FILM COATED in 1 BOTTLE (59762-0119-1)
Annotations
UNII (FDA Substance ID)
2681D7P965
PHENELZINE SULFATE
RxCUI 8124
Orange Book
N011909
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2681D7P965",
"rxcui": "8124",
"inchikey": "RXBKMJIPNDOHFR-UHFFFAOYSA-N",
"display_name": "PHENELZINE SULFATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"fa041652-fdde-4794-a8d2-279dd309e075": {
"match": "brand_token",
"title": "PHENELZINE SULFATE TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.]",
"spl_version": "14",
"published_date": "2026-05-25"
}
},
"productid": "59762-0119_d7302106-710a-49a4-9ab4-2de28937306c",
"productndc": "59762-0119",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "011909",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "EQ 15MG BASE",
"product_no": "002",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PHENELZINE SULFATE",
"proprietary_name": "phenelzine sulfate",
"active_ingred_unit": "mg/1",
"application_number": "NDA011909",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "Phenelzine Sulfate",
"start_marketing_date": "20110323",
"active_numerator_strength": "15"
}Related drugs
Other records sharing ATC code N06AF.
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