NDC product
Ibuprofen and Pseudoephedrine Hydrochloride
NDC 11822-0084 · Rite-Aid
Key facts
| Product NDC | 11822-0084 |
|---|---|
| Proprietary name | Ibuprofen and Pseudoephedrine Hydrochloride |
| Nonproprietary name | Ibuprofen and Pseudoephedrine Hydrochloride |
| Substances | IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE |
| Dosage form | TABLET, COATED |
| Route | ORAL |
| Labeler | Rite-Aid |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA074567 |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC] |
| Marketing start | Feb 1, 2018 |
| 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: