NDC 10267-3579 – Cetirizine Hydrochloride 10 mg
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC10267-3579
Product details
- Brand name
- Cetirizine Hydrochloride 10 mg
- Generic name
- Cetirizine Hydrochloride 10 mg
- Labeler
- Contract Pharmacal Corp.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076047
- Marketed since
- April 16, 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 10 mg →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 10267-3579-1 | 1 BOTTLE in 1 CARTON (10267-3579-1) / 100 TABLET, FILM COATED in 1 BOTTLE | Dec 31, 2025 |
| 10267-3579-3 | 1 BOTTLE in 1 CARTON (10267-3579-3) / 30 TABLET, FILM COATED in 1 BOTTLE | Dec 31, 2025 |
| 10267-3579-4 | 100 TABLET, FILM COATED in 1 BOTTLE (10267-3579-4) | May 31, 2025 |
| 10267-3579-6 | 365 TABLET, FILM COATED in 1 BOTTLE (10267-3579-6) | Apr 16, 2025 |
| 10267-3579-7 | 1 BOTTLE in 1 CARTON (10267-3579-7) / 60 TABLET, FILM COATED in 1 BOTTLE | Dec 31, 2025 |