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Famotidine

NDC 58602-706 · Aurohealth LLC

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

Packages

58602-706-14 1 BOTTLE in 1 CARTON (58602-706-14) / 50 TABLET, FILM COATED in 1 BOTTLE

58602-706-15 2 BLISTER PACK in 1 CARTON (58602-706-15) / 8 TABLET, FILM COATED in 1 BLISTER PACK

58602-706-16 1 BOTTLE in 1 CARTON (58602-706-16) / 65 TABLET, FILM COATED in 1 BOTTLE

58602-706-18 1 BOTTLE in 1 CARTON (58602-706-18) / 80 TABLET, FILM COATED in 1 BOTTLE

58602-706-19 1 BOTTLE in 1 CARTON (58602-706-19) / 90 TABLET, FILM COATED in 1 BOTTLE

58602-706-21 1 BOTTLE in 1 CARTON (58602-706-21) / 100 TABLET, FILM COATED in 1 BOTTLE

58602-706-34 1 BOTTLE in 1 CARTON (58602-706-34) / 200 TABLET, FILM COATED in 1 BOTTLE

58602-706-39 1 BOTTLE in 1 CARTON (58602-706-39) / 365 TABLET, FILM COATED in 1 BOTTLE

58602-706-40 1 BOTTLE in 1 CARTON (58602-706-40) / 500 TABLET, FILM COATED in 1 BOTTLE

58602-706-41 1000 TABLET, FILM COATED in 1 BOTTLE (58602-706-41)

58602-706-44 1 BOTTLE in 1 CARTON (58602-706-44) / 400 TABLET, FILM COATED in 1 BOTTLE

58602-706-47 1 BOTTLE in 1 CARTON (58602-706-47) / 75 TABLET, FILM COATED in 1 BOTTLE

58602-706-50 1 BOTTLE in 1 CARTON (58602-706-50) / 85 TABLET, FILM COATED in 1 BOTTLE

58602-706-53 1 BOTTLE in 1 CARTON (58602-706-53) / 25 TABLET, FILM COATED in 1 BOTTLE

58602-706-54 1 BOTTLE in 1 CARTON (58602-706-54) / 70 TABLET, FILM COATED in 1 BOTTLE

58602-706-56 1 BOTTLE in 1 CARTON (58602-706-56) / 35 TABLET, FILM COATED in 1 BOTTLE

58602-706-62 5 BLISTER PACK in 1 CARTON (58602-706-62) / 5 TABLET, FILM COATED in 1 BLISTER PACK (58602-706-60)

58602-706-79 1 BLISTER PACK in 1 CARTON (58602-706-79) / 8 TABLET, FILM COATED in 1 BLISTER PACK

58602-706-88 750 TABLET, FILM COATED in 1 BOTTLE (58602-706-88)

58602-706-94 100 TABLET, FILM COATED in 1 BOTTLE (58602-706-94)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-665 — famotidine, 55910-808 — famotidine, calcium carbonate and magnesium hydroxide, 55910-814 — famotidine, 56062-088 — Famotidine, 56062-141 — Famotidine, 56062-194 — Famotidine, 56062-263 — famotidine, calcium carbonate and magnesium hydroxide, 57896-317 — Famotidine, 57896-319 — Famotidine, 58602-705 — Famotidine, 58602-828 — Famotidine, 58602-829 — Famotidine, 58602-859 — Famotidine, 59640-001 — famotidine, 59640-023 — famotidine, 59651-701 — FAMOTIDINE, 59651-908 — Ibuprofen and famotidine, 59779-141 — Famotidine, 59779-194 — Famotidine, 59779-738 — famotidine, calcium carbonate and magnesium hydroxide, +401 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels