Betaxolol Hydrochloride 61314-0245-02

Package NDC

61314-0245-02

Manufacturer: Sandoz Inc
Dosage Form: Solution/ Drops
Route: Ophthalmic
Product Type: Human Prescription Drug
Marketing Start: May 15, 2000
Listing Expires: December 31, 2026
Application: NDA019270

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Active Ingredients

Ingredient	Strength
Betaxolol Hydrochloride	5.6 mg/mL

Drug Class

Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]

Selected Package

61314-0245-02Selected

1 BOTTLE, PLASTIC in 1 CARTON (61314-245-02) / 15 mL in 1 BOTTLE, PLASTIC

Other packages for this product(2)

61314-0245-01

1 BOTTLE, PLASTIC in 1 CARTON (61314-245-01) / 5 mL in 1 BOTTLE, PLASTIC

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61314-0245-03

1 BOTTLE, PLASTIC in 1 CARTON (61314-245-03) / 10 mL in 1 BOTTLE, PLASTIC

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