NDC 49483-692 – Cetirizine Hydrochloride Tablets,10 mg
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC49483-692
Product details
- Brand name
- Cetirizine Hydrochloride Tablets,10 mg
- Generic name
- Cetirizine Hydrochloride
- Labeler
- TIME CAP LABORATORIES, INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078933
- Marketed since
- February 12, 2022
- 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 Tablets,10 mg →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 49483-692-01 | 100 TABLET in 1 BOTTLE (49483-692-01) | Mar 11, 2024 |
| 49483-692-20 | 200 TABLET in 1 BOTTLE (49483-692-20) | Mar 11, 2024 |
| 49483-692-50 | 500 TABLET in 1 BOTTLE (49483-692-50) | May 30, 2022 |
| 49483-692-65 | 365 TABLET in 1 BOTTLE (49483-692-65) | Feb 12, 2022 |