Cetirizine Hydrochloride 16571-0134
Product NDC
16571-0134- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 16, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA090191
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 1 mg/mL |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(2)
120 mL in 1 BOTTLE, PLASTIC (16571-134-12)
480 mL in 1 BOTTLE, PLASTIC (16571-134-48)