NDC product
Fluticasone Propionate and Salmeterol
NDC 0093-3607 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0093-3607 |
|---|---|
| Proprietary name | Fluticasone Propionate and Salmeterol |
| Nonproprietary name | Fluticasone Propionate and Salmeterol |
| Substances | FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE |
| Dosage form | POWDER, METERED |
| Route | RESPIRATORY (INHALATION) |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA208799 |
| Pharmacologic classes | Adrenergic beta2-Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], beta2-Adrenergic Agonist [EPC] |
| Marketing start | Apr 28, 2017 |
| 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: