NDC product
BIO SPECTRA ATTITUDE
NDC 61649-731 · 9055-7588 Québec Inc. DBA Attitude
Key facts
| Product NDC | 61649-731 |
|---|---|
| Proprietary name | BIO SPECTRA |
| Nonproprietary name | Sodium fluoride |
| Substances | SODIUM FLUORIDE |
| Dosage form | GEL, DENTIFRICE |
| Route | DENTAL |
| Labeler | 9055-7588 Québec Inc. DBA Attitude |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M021 |
| Marketing start | May 15, 2021 |
| Listing certified through | 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 · Source date: