NDC product
RYMED
NDC 0485-0080 · EDWARDS PHARMACEUTICALS, INC.
Key facts
| Product NDC | 0485-0080 |
|---|---|
| Proprietary name | RYMED |
| Nonproprietary name | DEXCHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
| Substances | DEXCHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage form | TABLET, COATED |
| Route | ORAL |
| Labeler | EDWARDS PHARMACEUTICALS, INC. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
| Marketing start | Nov 15, 2011 |
| 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: