Propranolol 51662-1700-01

Package NDC

51662-1700-01

Manufacturer: Hf Acquisition Co Llc, Dba Healthfirst
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: September 7, 2001
Listing Expires: December 31, 2027
Application: ANDA075826

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Active Ingredients

Ingredient	Strength
Propranolol Hydrochloride	1 mg/mL

Drug Class

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

Selected Package

51662-1700-01Selected

1 mL in 1 VIAL, SINGLE-DOSE (51662-1700-1)