Famotidine Tablets, Usp

SPL v3

SPL

SPL Set ID 8c17f9e3-9827-4bf9-85ca-72e08a8518ca

Route

ORAL

Published

Effective Date 2022-10-03

Document Type 34391-3 HUMAN PRESCRIPTION DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients

Famotidine (20 mg)

Inactive Ingredients

Hypromellose 2910 (5 Mpa.s) Hypromellose 2910 (6 Mpa.s) Magnesium Stearate Microcrystalline Cellulose 101 Microcrystalline Cellulose 102 Polyethylene Glycol 8000 Silicon Dioxide Sodium Starch Glycolate Type A Starch, Corn Talc Titanium Dioxide

Identifiers & Packaging

Pill Appearance

Imprint: Z41 Shape: round Color: white Size: 6 mm Size: 8 mm Score: 1

Marketing Status

ANDA Active Since 2022-06-06

Description

NDC 70771-1702-3 Famotidine Tablets USP, 20 mg 30 Tablets Rx only NDC 70771-1703-3 Famotidine Tablets USP, 40 mg 30 Tablets Rx only

Medication Information

Description

NDC 70771-1702-3 Famotidine Tablets USP, 20 mg 30 Tablets Rx only NDC 70771-1703-3 Famotidine Tablets USP, 40 mg 30 Tablets Rx only

Package Label.principal Display Panel

NDC 70771-1702-3

Famotidine Tablets USP, 20 mg

30 Tablets

Rx only

NDC 70771-1703-3

Famotidine Tablets USP, 40 mg

30 Tablets

Rx only

Structured Label Content

Package Label.principal Display Panel (PACKAGE LABEL.PRINCIPAL DISPLAY PANEL)

NDC 70771-1702-3

Famotidine Tablets USP, 20 mg

30 Tablets

Rx only

NDC 70771-1703-3

Famotidine Tablets USP, 40 mg

30 Tablets

Rx only

Advanced Ingredient Data

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Raw Label Data

All Sections (JSON)

{"PACKAGE LABEL.PRINCIPAL DISPLAY PANEL": "NDC 70771-1702-3 Famotidine Tablets USP, 20 mg 30 Tablets Rx only NDC 70771-1703-3 Famotidine Tablets USP, 40 mg 30 Tablets Rx only"}

Additional Information

Back to search View SPL set listing Open on DailyMed ↗

Source: dailymed · Ingested: 2026-02-15T11:43:58.964040 · Updated: 2026-03-14T22:18:18.443233