United States · FDA National Drug Code directory

Maximum Strength Acid Reducer

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
49483-720_12f9b308-9375-2df3-e063-6394a90a8d22
Product NDC
49483-720
Form
TABLET
Composition / generic term
Famotidine
Labeler
TIME CAP LABORATORIES,INC
Marketing category
ANDA
Marketing start / end (source format)
20230615
Source listing expiry
20261231

Source-listed ingredients

  • FAMOTIDINE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (49483-720-01) · 49483-720-01
  • 200 TABLET in 1 BOTTLE (49483-720-20) · 49483-720-20

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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