NDC product
Lidocaine
NDC 0362-0262 · Septodont, Inc.
Key facts
| Product NDC | 0362-0262 |
|---|---|
| Proprietary name | Lidocaine |
| Nonproprietary name | Lidocaine Hydrochloride and Epinephrine |
| Substances | LIDOCAINE HYDROCHLORIDE, EPINEPHRINE BITARTRATE |
| Dosage form | INJECTION, SOLUTION |
| Route | SUBMUCOSAL |
| Labeler | Septodont, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA088389 |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Catecholamine [EPC] and 4 more |
| Marketing start | Aug 10, 2018 |
| 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: