NDC 72162-2173 – cetirizine hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-2173
Product details
- Brand name
- cetirizine hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078336
- Marketed since
- December 27, 2007
- 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 →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72162-2173-2 | 1 BOTTLE in 1 CARTON (72162-2173-2) / 300 TABLET, FILM COATED in 1 BOTTLE | Jan 23, 2024 |
| 72162-2173-3 | 1 BOTTLE in 1 CARTON (72162-2173-3) / 30 TABLET, FILM COATED in 1 BOTTLE | Jun 18, 2024 |
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