NDC 85509-1315 – Ibuprofen And Famotidine

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

Human Prescription Drug

Product NDC85509-1315

Product details

Brand name
Ibuprofen And Famotidine
Generic name
Ibuprofen and famotidine
Labeler
PHOENIX RX LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216814
Marketed since
March 15, 2023
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
85509-1315-330 TABLET in 1 BOTTLE (85509-1315-3)Sep 29, 2025
85509-1315-660 TABLET in 1 BOTTLE (85509-1315-6)Sep 29, 2025
85509-1315-990 TABLET in 1 BOTTLE (85509-1315-9)Sep 29, 2025

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