NDC 0781-1684 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC0781-1684
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Sandoz Inc
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077946
- 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 |
|---|---|---|
| 0781-1684-01 | 100 TABLET in 1 BOTTLE (0781-1684-01) | Dec 27, 2007 |
| 0781-1684-64 | 30 TABLET in 1 BOX, UNIT-DOSE (0781-1684-64) | Dec 27, 2007 |
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