Azelastine Hydrochloride 47335-0938
Product NDC
47335-0938- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Solution/ Drops
- Route
- Intraocular
- Product Type
- Human Prescription Drug
- Marketing Start
- May 31, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA078738
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Azelastine Hydrochloride | .5 mg/mL |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
1 BOTTLE, PLASTIC in 1 BOX (47335-938-90) / 6 mL in 1 BOTTLE, PLASTIC