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United States · US · US:43386-360_1eb0b695-ce65-45c2-914a-87bc2105b139
Phenelzine Sulfate
Orange BookUNIISPLATC N06AF
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLupin Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeN06AF
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11433863602160 TABLET in 1 BOTTLE (43386-360-21)
Annotations
UNII (FDA Substance ID)
2681D7P965
PHENELZINE SULFATE
RxCUI 8124
Orange Book
A200181
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": "43386-360_1eb0b695-ce65-45c2-914a-87bc2105b139",
"productndc": "43386-360",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "200181",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 15MG BASE",
"product_no": "001",
"approval_date": "Dec 8, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PHENELZINE SULFATE",
"proprietary_name": "Phenelzine Sulfate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA200181",
"marketing_category": "ANDA",
"nonproprietary_name": "Phenelzine Sulfate",
"start_marketing_date": "20101214",
"active_numerator_strength": "15"
}Related drugs
Other records sharing ATC code N06AF.
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