NDC 51672-2106 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 1 mg/mL · Solution · Oral
Product NDC51672-2106
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA201546
- Marketed since
- May 20, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 1 mg/mL
Uses, dosage, side effects and warnings for Cetirizine hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-2106-1 | 1 BOTTLE in 1 CARTON (51672-2106-1) / 240 mL in 1 BOTTLE | May 20, 2011 |
| 51672-2106-4 | 1 BOTTLE in 1 CARTON (51672-2106-4) / 60 mL in 1 BOTTLE | May 20, 2011 |
| 51672-2106-8 | 1 BOTTLE in 1 CARTON (51672-2106-8) / 120 mL in 1 BOTTLE | May 20, 2011 |
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