NDC 51655-194 – Cetirizine
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-194
Product details
- Brand name
- Cetirizine
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078336
- Marketed since
- October 18, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 10 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51655-194-26 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-26) | Nov 15, 2022 |
| 51655-194-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-52) | Mar 2, 2023 |
| 51655-194-60 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-194-60) | Oct 18, 2022 |
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