NDC 85509-1010 – Ibuprofen and famotidine

Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC85509-1010

Product details

Brand name
Ibuprofen and famotidine
Generic name
Ibuprofen and famotidine
Labeler
PHOENIX RX LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211890
Marketed since
August 4, 2021
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
85509-1010-330 TABLET, FILM COATED in 1 BOTTLE (85509-1010-3)Jul 21, 2025
85509-1010-660 TABLET, FILM COATED in 1 BOTTLE (85509-1010-6)Jul 21, 2025
85509-1010-990 TABLET, FILM COATED in 1 BOTTLE (85509-1010-9)Jul 21, 2025

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