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berkley and jensen famotidine

NDC 68391-300 · BJWC

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

68391-300-82 — 2 BOTTLE in 1 PACKAGE (68391-300-82) / 100 TABLET, FILM COATED in 1 BOTTLE

68391-300-85 — 2 BOTTLE in 1 PACKAGE (68391-300-85) / 125 TABLET, FILM COATED in 1 BOTTLE (68391-300-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3413 — FAMOTIDINE, 68071-3420 — FAMOTIDINE, 68071-3521 — Famotidine, 68071-3584 — FAMOTIDINE, 68071-3786 — Famotidine, 68071-4197 — Famotidine, 68094-054 — FAMOTIDINE, 68180-150 — Famotidine, 68196-121 — Famotidine, 68382-444 — famotidine, 68475-400 — famotidine, 68645-594 — Famotidine, 68788-4021 — Famotidine, 68788-4088 — Famotidine, 68788-4119 — Famotidine, 68788-4144 — Famotidine, 68788-8485 — FAMOTIDINE, 68788-8518 — FAMOTIDINE, 68788-8733 — Famotidine, 68788-8889 — 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.