NDC 80425-0483 – Ibuprofen and famotidine

Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC80425-0483

Product details

Brand name
Ibuprofen and famotidine
Generic name
Ibuprofen and famotidine
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203658
Marketed since
March 22, 2024
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen And Famotidine →

Package NDC codes (3)

Package NDCDescriptionSince
80425-0483-130 TABLET in 1 BOTTLE (80425-0483-1)Mar 22, 2024
80425-0483-260 TABLET in 1 BOTTLE (80425-0483-2)Mar 22, 2024
80425-0483-390 TABLET in 1 BOTTLE (80425-0483-3)Mar 22, 2024

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