NDC product
ADVIL ALLERGY SINUS
NDC 0573-0188 · Haleon US Holdings LLC
Key facts
| Product NDC | 0573-0188 |
|---|---|
| Proprietary name | ADVIL ALLERGY SINUS |
| Nonproprietary name | chlorpheniramine maleate, ibuprofen, pseudoephedrine HCl |
| Substances | CHLORPHENIRAMINE MALEATE, IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE |
| Dosage form | TABLET, COATED |
| Route | ORAL |
| Labeler | Haleon US Holdings LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | NDA |
| Application number | NDA021441 |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] and 2 more |
| Marketing start | Dec 20, 2002 |
| 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: