Azelastine Hydrochloride 61314-0308-02

Package NDC

61314-0308-02

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]

Selected Package

61314-0308-02Selected

1 BOTTLE, PLASTIC in 1 CARTON (61314-308-02) / 6 mL in 1 BOTTLE, PLASTIC