NDC 16571-134 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 1 mg/mL · Solution · Oral
Product NDC16571-134
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA090191
- Marketed since
- July 16, 2024
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 16571-134-12 | 120 mL in 1 BOTTLE, PLASTIC (16571-134-12) | Jul 16, 2024 |
| 16571-134-48 | 480 mL in 1 BOTTLE, PLASTIC (16571-134-48) | Jul 16, 2024 |
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