NDC 45802-919 – Cetirizine hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC45802-919
Product details
- Brand name
- Cetirizine hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- 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 |
|---|---|---|
| 45802-919-39 | 1 BOTTLE in 1 CARTON (45802-919-39) / 30 TABLET, FILM COATED in 1 BOTTLE | Oct 15, 2008 |
| 45802-919-87 | 1 BOTTLE in 1 CARTON (45802-919-87) / 300 TABLET, FILM COATED in 1 BOTTLE | Dec 27, 2007 |
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