Esmolol Hydrochloride 10019-0120

Product NDC

10019-0120

Manufacturer: Baxter Healthcare Corporation
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: December 31, 1986
Listing Expires: December 31, 2027
Application: NDA019386

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Active Ingredients

Ingredient	Strength
Esmolol Hydrochloride	10 mg/mL

Drug Class

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

Packaging Options(1)

10019-0120-01

25 VIAL in 1 CARTON (10019-120-01) / 10 mL in 1 VIAL (10019-120-39)

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