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United States · US · US:0071-0350_87512ea9-1c68-4ec1-a8d0-37776f006227
Nardil
Orange BookUNIISPLATC N06AF
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerParke-Davis Div of Pfizer Inc
CountryUS (United States)
ATC codeN06AF
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11007103506060 TABLET, FILM COATED in 1 BOTTLE (0071-0350-60)
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": {
"513a41d0-37d4-4355-8a6d-a2c643bce6fa": {
"match": "brand_token",
"title": "NARDIL (PHENELZINE SULFATE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]",
"spl_version": "11",
"published_date": "2025-06-09"
}
},
"productid": "0071-0350_87512ea9-1c68-4ec1-a8d0-37776f006227",
"productndc": "0071-0350",
"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": "Nardil",
"active_ingred_unit": "mg/1",
"application_number": "NDA011909",
"marketing_category": "NDA",
"nonproprietary_name": "Phenelzine Sulfate",
"start_marketing_date": "19610609",
"active_numerator_strength": "15"
}Related drugs
Other records sharing ATC code N06AF.
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