NDC 51655-842 – Cetirizine Hydrochloride Tablets,10 mg
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC51655-842
Product details
- Brand name
- Cetirizine Hydrochloride Tablets,10 mg
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078933
- Marketed since
- February 7, 2023
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 51655-842-26 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-842-26) | Feb 7, 2023 |
| 51655-842-52 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-842-52) | Apr 7, 2023 |
| 51655-842-60 | 100 TABLET in 1 BOTTLE, PLASTIC (51655-842-60) | Mar 30, 2023 |
| 51655-842-84 | 14 TABLET in 1 BOTTLE, PLASTIC (51655-842-84) | Mar 10, 2023 |