NDC 67877-626 – Ibuprofen and famotidine

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

Human Prescription Drug 1 recall

Product NDC67877-626

Product details

Brand name
Ibuprofen and famotidine
Generic name
Ibuprofen and famotidine
Labeler
Ascend Laboratories, LLC
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 (4)

Package NDCDescriptionSince
67877-626-01100 TABLET, FILM COATED in 1 BOTTLE (67877-626-01)Aug 4, 2021
67877-626-05500 TABLET, FILM COATED in 1 BOTTLE (67877-626-05)Aug 4, 2021
67877-626-066 BLISTER PACK in 1 CARTON (67877-626-06) / 1 TABLET, FILM COATED in 1 BLISTER PACKAug 4, 2021
67877-626-9090 TABLET, FILM COATED in 1 BOTTLE (67877-626-90)Aug 4, 2021

Recalls mentioning this NDC

Other Ibuprofen And Famotidine products