NDC 72789-458 – Cetirizine hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-458
Product details
- Brand name
- Cetirizine hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076047
- Marketed since
- April 23, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cetirizine hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 72789-458-10 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-458-10) | Oct 23, 2025 |
| 72789-458-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-458-30) | May 29, 2025 |
| 72789-458-51 | 365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-458-51) | Apr 23, 2025 |
| 72789-458-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-458-90) | May 29, 2025 |
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