NDC product
Benzonatate
NDC 55154-3372 · Cardinal Health 107, LLC
Key facts
| Product NDC | 55154-3372 |
|---|---|
| Proprietary name | Benzonatate |
| Nonproprietary name | Benzonatate |
| Substances | BENZONATATE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Cardinal Health 107, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA206948 |
| Pharmacologic classes | Decreased Tracheobronchial Stretch Receptor Activity [PE], Non-narcotic Antitussive [EPC] |
| Marketing start | Dec 21, 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: