NDC product
Tizanidne hydrochloride
NDC 72162-1860 · Bryant Ranch Prepack
Key facts
| Product NDC | 72162-1860 |
|---|---|
| Proprietary name | Tizanidne hydrochloride |
| Nonproprietary name | Tizanidne hydrochloride |
| Substances | TIZANIDINE HYDROCHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Bryant Ranch Prepack |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA212196 |
| Pharmacologic classes | Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC] |
| Marketing start | Mar 29, 2019 |
| 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: