phenelzine sulfate
- Product NDC
- 59762-0119
- 11-digit product format
- 597620119
- Labeler code
- 59762
- Product ID
- 59762-0119_d7302106-710a-49a4-9ab4-2de28937306c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenelzine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- NDA011909
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2011-03-23
- Substance
- PHENELZINE SULFATE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Monoamine Oxidase Inhibitor [EPC], Monoamine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- phenelzine sulfate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENELZINE SULFATE | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2681D7P965 |
| Rxcui | 312347 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59762-0119-1 | phenelzine sulfate | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 14 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| 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 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| 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 RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59762-0119-1 | 59762011901 | 60 TABLET, FILM COATED in 1 BOTTLE (59762-0119-1) | 2011-03-23 | 0000-00-00 | No | No | Current |