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Furosemide

NDC 68071-3673 · NuCare 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

68071-3673-3 — 30 TABLET in 1 BOTTLE (68071-3673-3)

68071-3673-9 — 90 TABLET in 1 BOTTLE (68071-3673-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1555 — Furosemide, 67046-1589 — Furosemide, 67046-1663 — Furosemide, 67296-2136 — Furosemide, 67296-2139 — Furosemide, 68071-1708 — Furosemide, 68071-1809 — Furosemide, 68071-2360 — furosemide, 68071-3273 — Furosemide, 68071-3536 — Furosemide, 68071-4445 — furosemide, 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, +194 more

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