NDC product
phenelzine sulfate
NDC 59762-0119 · Mylan Pharmaceuticals Inc.
Key facts
| Product NDC | 59762-0119 |
|---|---|
| Proprietary name | phenelzine sulfate |
| Nonproprietary name | Phenelzine Sulfate |
| Substances | PHENELZINE SULFATE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Mylan Pharmaceuticals Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA011909 |
| Pharmacologic classes | Monoamine Oxidase Inhibitor [EPC], Monoamine Oxidase Inhibitors [MoA] |
| Marketing start | Mar 23, 2011 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: