NDC product
Fluticasone Propionate
NDC 49035-362 · Walmart
Key facts
| Product NDC | 49035-362 |
|---|---|
| Proprietary name | Fluticasone Propionate |
| Nonproprietary name | Fluticasone Propionate |
| Substances | FLUTICASONE PROPIONATE |
| Dosage form | SPRAY, METERED |
| Route | NASAL |
| Labeler | Walmart |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA208150 |
| Pharmacologic classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| Marketing start | Oct 23, 2017 |
| Marketing end | Oct 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