Furosemide 71288-0203

Product NDC

71288-0203

Manufacturer: Meitheal Pharmaceuticals Inc.
Dosage Form: Injection, Solution
Route: Intramuscular And Intravenous
Product Type: Human Prescription Drug
Marketing Start: January 27, 2022
Listing Expires: December 31, 2026
Application: ANDA212803

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Active Ingredients

Ingredient	Strength
Furosemide	10 mg/mL

Drug Class

Loop Diuretic [EPC]Increased Diuresis at Loop of Henle [PE]Loop Diuretic [EPC]

Packaging Options(2)

71288-0203-92

25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-92) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-203-91)

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71288-0203-94

25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-94) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-203-93)

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