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Ranitidine

NDC 0121-4727 · Pharmaceutical Associates, Inc.

Generic nameRANITIDINE
Dosage formSYRUP
RouteORAL
Active ingredient(s)RANITIDINE
Strength15 mg/mL
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

0121-4727-10 — 4 TRAY in 1 CASE (0121-4727-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0121-0727 — RANITIDINE

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