NDC 69306-266 – Ibuprofen and famotidine

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

Human Prescription Drug

Product NDC69306-266

Product details

Brand name
Ibuprofen and famotidine
Generic name
Ibuprofen and famotidine
Labeler
Doc Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211890
Marketed since
August 4, 2021
Listing expires
December 31, 2027
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
69306-266-3030 TABLET, FILM COATED in 1 BOTTLE (69306-266-30)Aug 30, 2022
69306-266-6060 TABLET, FILM COATED in 1 BOTTLE (69306-266-60)Aug 1, 2026
69306-266-9090 TABLET, FILM COATED in 1 BOTTLE (69306-266-90)Aug 1, 2026

Other Ibuprofen And Famotidine products