DailyMed label

Famotidine

DailyMed label · Proficient Rx LP · version 8

Key facts

Product Famotidine
Labeler Proficient Rx LP
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients FAMOTIDINE
Active ingredient UNIIs 5QZO15J2Z8
Application number 075511
Route ORAL
NDC package codes 71205-276-06, 71205-276-10, 71205-276-30, 71205-276-60, 71205-276-90, 71205-276-78, 71205-276-67
Effective date Mar 1, 2026
Set ID d60bde93-f512-4071-9e4b-1d8318def3bc

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • 1–9 Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About DailyMed drug labels

DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

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