NDC product
Nortriptyline Hydrochloride
NDC 70710-1156 · Zydus Pharmaceuticals (USA) Inc.
Key facts
| Product NDC | 70710-1156 |
|---|---|
| Proprietary name | Nortriptyline Hydrochloride |
| Nonproprietary name | Nortriptyline Hydrochloride |
| Substances | NORTRIPTYLINE HYDROCHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Zydus Pharmaceuticals (USA) Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA213441 |
| Pharmacologic classes | Tricyclic Antidepressant [EPC] |
| Marketing start | Feb 10, 2022 |
| 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: