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Furosemide

NDC 68788-8870 · Prefferred Pharmaceuticals Inc.

Generic nameFurosemide
Dosage formTABLET
RouteORAL
Active ingredient(s)FUROSEMIDE
Strength20 mg/1
Pharmacologic classIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
Marketing categoryANDA

Packages

68788-8870-1 — 100 TABLET in 1 BOTTLE (68788-8870-1)

68788-8870-3 — 30 TABLET in 1 BOTTLE (68788-8870-3)

68788-8870-6 — 60 TABLET in 1 BOTTLE (68788-8870-6)

68788-8870-9 — 90 TABLET in 1 BOTTLE (68788-8870-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-4522 — furosemide, 68071-4534 — furosemide, 68083-432 — Furosemide, 68083-433 — Furosemide, 68083-434 — Furosemide, 68094-756 — Furosemide, 68094-867 — Furosemide, 68788-6784 — Furosemide, 68788-6948 — Furosemide, 68788-8799 — Furosemide, 69315-116 — Furosemide, 69315-117 — Furosemide, 69315-118 — Furosemide, 70121-1076 — Furosemide, 70121-1163 — Furosemide, 70121-1164 — Furosemide, 70518-0050 — Furosemide, 70518-0251 — Furosemide, 70518-2528 — Furosemide, 70518-3061 — furosemide, +194 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.