NDC 51655-801 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-801
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride Tablets
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078343
- Marketed since
- January 25, 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 →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51655-801-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-52) | Jan 25, 2023 |
| 51655-801-60 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-60) | Jan 25, 2023 |
| 51655-801-84 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-84) | Jan 25, 2023 |
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