Ibuprofen And Famotidine Tablets

SPL v1

SPL

SPL Set ID 24204938-0989-42ad-8ad8-89979e62d700

Route

ORAL

Published

Effective Date 2025-05-28

Document Type 34391-3 HUMAN PRESCRIPTION DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients

Ibuprofen (800 mg) Famotidine (26.6 mg)

Inactive Ingredients

Croscarmellose Sodium Ferrosoferric Oxide Glyceryl Mono- And Dicaprylocaprate Hypromellose 2910 (15 Mpa.s) Magnesium Stearate Microcrystalline Cellulose Polyvinyl Alcohol, Unspecified Propylene Glycol Shellac Silicon Dioxide Sodium Lauryl Sulfate Talc Titanium Dioxide

Identifiers & Packaging

Pill Appearance

Imprint: 777 Shape: capsule Color: white Size: 18 mm Score: 1

Marketing Status

ANDA Active Since 2025-06-01

Description

Ibuprofen and famotidine tablets, 800 mg/26.6 mg 90 Tablets NDC 70771-1924-9 Rx only

Medication Information

Description

Ibuprofen and famotidine tablets, 800 mg/26.6 mg 90 Tablets NDC 70771-1924-9 Rx only

Package Label.principal Display Panel

Ibuprofen and famotidine tablets, 800 mg/26.6 mg

90 Tablets

NDC 70771-1924-9

Rx only

Structured Label Content

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

Ibuprofen and famotidine tablets, 800 mg/26.6 mg

90 Tablets

NDC 70771-1924-9

Rx only

Advanced Ingredient Data

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Raw Label Data

All Sections (JSON)

{"PACKAGE LABEL.PRINCIPAL DISPLAY PANEL": "Ibuprofen and famotidine tablets, 800 mg/26.6 mg 90 Tablets NDC 70771-1924-9 Rx only"}

Additional Information

Back to search View SPL set listing Open on DailyMed ↗

Source: dailymed · Ingested: 2026-02-15T11:47:22.532882 · Updated: 2026-03-14T22:27:03.737378