NDC 59762-0119-01 - phenelzine sulfate
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 59762-0119
- Requested NDC
- 59762-0119-01
- Package NDCs from labels
- 59762-0119-1, 59762-0119-01
- Manufacturer
- Mylan Pharmaceuticals Inc.
- Effective date
- 2026-05-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PHENELZINE SULFATE Tablets, USP | Mylan Pharmaceuticals Inc. | 2026-05-21 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59762-0119-1 | phenelzine sulfate | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 14 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59762-0119 | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 10 | Current NDC, Legacy NDC, 1 package rows | 20250221_fa041652-fdde-4794-a8d2-279dd309e075.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 59762-0119-1 | EA - Each | 59762-0119 | 5d9afadc-06e6-4074-8a76-602029893008 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| PHENELZINE SULFATE | ACTIVE INGREDIENT | 2681D7P965 | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| PHENELZINE | ACTIVE MOIETY | O408N561GF | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| EDETATE DISODIUM | INACTIVE INGREDIENT | 7FLD91C86K | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| ISOPROPYL ALCOHOL | INACTIVE INGREDIENT | ND2M416302 | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | PHENELZINE SULFATE TABLET, FILM COATED [GREENSTONE LLC] | 4 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ALCOHOL PREP PADS LARGE STERILE | ISOPROPYL ALCOHOL CLOTH | JINHUA JINGDI MEDICAL SUPPLIES CO.,LTD | 4f8ba6c8-5155-c491-e063-6394a90adde9 | 2026-04-15 | Warnings | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Perrigo Direct, Inc | ec43a3f5-c5f3-439b-8764-ca92fefb45c9 | 2026-04-10 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | MSC Industrial Supply | b248ad4a-ed92-4d03-b0da-9639c46e1949 | 2026-04-10 | Warnings, Adverse reactions | ND2M416302 |
| Verifine Alcohol Swabs | ALCOHOL SWABS | Promisemed Hangzhou Meditech Co.,LTD. | 4ef56b6c-ad46-2d02-e063-6294a90ad407 | 2026-04-08 | Warnings | ND2M416302 |
| FreshKote Preservative Free Lubricant Eye Drops | POVIDONE, POLYVINYL ALCOHOL | Eyevance Pharmaceuticals | f51c50c3-43ae-4169-9d2b-22b239461dd1 | 2026-04-08 | Warnings | FZ989GH94E |
| 70% | ISOPROPYL ALCOHOL | Perrigo Direct, Inc | f953a249-07ad-40a1-8aea-b2d419fd3d4d | 2026-04-07 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | WinCo Foods, LLC | c22a5fc3-78f5-4660-96a6-479ca6f77602 | 2026-04-06 | Warnings, Adverse reactions | ND2M416302 |
| 70% Isopropyl Rubbing Alcohol | ISOPROPYL RUBBING ALCOHOL | WinCo Foods, LLC | 2b48ee19-8f0c-4b36-855d-7909dde5c871 | 2026-04-06 | Warnings, Adverse reactions | ND2M416302 |
| 50% Rubbing | ISOPROPYL ALCOHOL | Perrigo Direct, Inc | 698bede7-4fc1-4e85-8ac4-d735f409cfae | 2026-04-06 | Warnings, Adverse reactions | ND2M416302 |
| KIDS TOOTHPASTE, FOR CAVITY PROTECTION | KIDS TOOTHPASTE FOR CAVITY PROTECTION | Shulisa (Foshan) Daily ChemicalIndustry Co., Ltd | 4e8fab9e-f05c-5e2f-e063-6294a90aecf9 | 2026-04-03 | Warnings | 059QF0KO0R |
| Medt Pad | ISOPROPYL ALCOHOL | Carelife (USA) Inc. | 74a05c37-becd-4c93-96cb-79f69add5e4d | 2026-04-02 | Warnings | ND2M416302 |
| Walgreens Swimmers Ear | ISOPROPYL ALCOHOL | Walgreens Co | 3fb65a5c-c47f-ef2b-e063-6394a90af21a | 2026-04-01 | Warnings | ND2M416302 |
| Isopro First Aid | ISOPROPYL ALCOHOL | Water-Jel Technologies | f38563f5-ee54-4979-9157-4bf8fd60daab | 2026-03-31 | Warnings | ND2M416302 |
| Verifine Alcohol Swabs | ALCOHOL SWABS | Promisemed Hangzhou Meditech Co.,LTD. | 4e404989-89d0-b189-e063-6394a90a8caa | 2026-03-30 | Warnings | ND2M416302 |
| MedPride Sterile Prep Pads | ISOPROPYL ALCOHOL | Shield Line LLC | 31de24d8-b70e-47f1-8946-6bd9fb16b5d5 | 2026-03-30 | Warnings | ND2M416302 |
| Swim-EAR | SWIM-EAR | Fougera Pharmaceuticals, LLC | b849acb5-e20b-464c-948b-8dcc51fdaf70 | 2026-03-26 | Warnings | ND2M416302 |
| THESIS PHARMACY Alcohol Prep Pad | ISOPROPYL ALCOHOL | Carelife (USA) Inc. | 841d8b55-6383-4e02-9047-7b01e9f20a54 | 2026-03-24 | Warnings | ND2M416302 |
| Sterile Water | WATER | Hospira, Inc. | 2b9ea23a-f9e9-48a8-25b7-519e3bbd6828 | 2026-03-18 | Warnings, Adverse reactions | 059QF0KO0R |
| TINTED SUNSCREEN FOUNDATION | TINTED SUNSCREEN FOUNDATION | Guanghzou AiXin Biotech Co Ltd | 396393c4-b50c-3877-e063-6294a90a0e9b | 2026-03-17 | Warnings | 059QF0KO0R |
| MedPRIDE | ISOPROPYL ALCOHOL | Shield Line LLC | f2177bd3-259d-4231-88b2-4a98e48e4df6 | 2026-03-17 | Warnings | ND2M416302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.