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Curist Acid Relief

NDC 72559-032 · Little Pharma, Inc.

Generic nameFamotidine 20 mg
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

72559-032-22 — 200 TABLET in 1 BOTTLE (72559-032-22)

72559-032-23 — 300 TABLET in 1 BOTTLE (72559-032-23)

72559-032-63 — 500 TABLET in 1 BOTTLE (72559-032-63)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72205-233 — FAMOTIDINE, 72288-141 — Famotidine, 72288-151 — famotidine, 72288-194 — Famotidine, 72288-321 — famotidine, calcium carbonate and magnesium hydroxide, 72288-329 — famotidine, 72288-363 — Famotidine, 72288-774 — famotidine, calcium carbonate and magnesium hydroxide, 72476-150 — famotidine, 72476-299 — famotidine, 72559-038 — Famotidine, 72578-214 — Ibuprofen and Famotidine, 72603-171 — Famotidine, 72657-112 — Famotidine, 72657-113 — Famotidine, 72657-132 — Famotidine, 72789-331 — Famotidine, 72789-345 — FAMOTIDINE, 72789-427 — Famotidine, 72789-453 — FAMOTIDINE, +401 more

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