Azelastine Hydrochloride 61314-0308
Product NDC
61314-0308- Manufacturer
- Sandoz Inc
- Dosage Form
- Solution/ Drops
- Route
- Intraocular
- Product Type
- Human Prescription Drug
- Marketing Start
- March 21, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA202305
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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 CARTON (61314-308-02) / 6 mL in 1 BOTTLE, PLASTIC