NDC product
Tiagabine Hydrochloride
NDC 72205-084 · Novadoz Pharmaceuticals LLC
Key facts
| Product NDC | 72205-084 |
|---|---|
| Proprietary name | Tiagabine Hydrochloride |
| Nonproprietary name | Tiagabine Hydrochloride |
| Substances | TIAGABINE HYDROCHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Novadoz Pharmaceuticals LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA214816 |
| Pharmacologic classes | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| Marketing start | Nov 23, 2021 |
| 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: