Azelastine Hydrochloride 47335-0779
Product NDC
47335-0779- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Spray, Metered
- Route
- Nasal
- Product Type
- Human Prescription Drug
- Marketing Start
- May 24, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA090423
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Azelastine Hydrochloride | 137 ug/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
1 BOTTLE, SPRAY in 1 BOX (47335-779-91) / 200 SPRAY, METERED in 1 BOTTLE, SPRAY