phenelzine sulfate

Generic: phenelzine sulfate

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name phenelzine sulfate
Generic Name phenelzine sulfate
Labeler mylan pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

phenelzine sulfate 15 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59762-0119
Product ID 59762-0119_a1789800-9bb6-42d3-967f-122f07c5b69c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA011909
Listing Expiration 2026-12-31
Marketing Start 2011-03-23

Pharmacologic Class

Classes
monoamine oxidase inhibitor [epc] monoamine oxidase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 597620119
Hyphenated Format 59762-0119

Supplemental Identifiers

RxCUI
312347
UPC
0359762011916
UNII
2681D7P965

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name phenelzine sulfate (source: ndc)
Generic Name phenelzine sulfate (source: ndc)
Application Number NDA011909 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (59762-0119-1)
source: ndc

Packages (1)

Ingredients (1)

phenelzine sulfate (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a1789800-9bb6-42d3-967f-122f07c5b69c", "openfda": {"upc": ["0359762011916"], "unii": ["2681D7P965"], "rxcui": ["312347"], "spl_set_id": ["fa041652-fdde-4794-a8d2-279dd309e075"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (59762-0119-1)", "package_ndc": "59762-0119-1", "marketing_start_date": "20110323"}], "brand_name": "phenelzine sulfate", "product_id": "59762-0119_a1789800-9bb6-42d3-967f-122f07c5b69c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Monoamine Oxidase Inhibitor [EPC]", "Monoamine Oxidase Inhibitors [MoA]"], "product_ndc": "59762-0119", "generic_name": "Phenelzine Sulfate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "phenelzine sulfate", "active_ingredients": [{"name": "PHENELZINE SULFATE", "strength": "15 mg/1"}], "application_number": "NDA011909", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20110323", "listing_expiration_date": "20261231"}