FDA NDC Directory · JSON-LD · Markdown
NDC 51316-607 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | Cetirizine hydrochloride, Pseudoephedrine hydrochloride |
|---|---|
| Labeler / Manufacturer | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
| Marketing category | Abbreviated NDA (generic) · App ANDA210719 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | CETIRIZINE HYDROCHLORIDE (5 mg/1) PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1) |
| Marketing started | 20251210 |
| Package count | 2 |
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