NDC product
Venlafaxine Hydrochloride
NDC 13811-712 · Trigen Laboratories, LLC
Key facts
| Product NDC | 13811-712 |
|---|---|
| Proprietary name | Venlafaxine Hydrochloride |
| Nonproprietary name | venlafaxine hydrochloride |
| Substances | VENLAFAXINE HYDROCHLORIDE |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Trigen Laboratories, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA022104 |
| Pharmacologic classes | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
| Marketing start | Apr 29, 2010 |
| Marketing end | Dec 31, 2026 |
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