NDC 55111-118 – Famotidine

Famotidine 10 mg/1 · Tablet · Oral

Human Otc Drug 1 recall

Product NDC55111-118

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Dr.Reddys Laboratories Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077367
Marketed since
September 30, 2006
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (11)

Package NDCDescriptionSince
55111-118-041 BOTTLE in 1 CARTON (55111-118-04) / 120 TABLET in 1 BOTTLEOct 1, 2020
55111-118-121 BLISTER PACK in 1 CARTON (55111-118-12) / 12 TABLET in 1 BLISTER PACKSep 30, 2006
55111-118-181 BOTTLE in 1 CARTON (55111-118-18) / 180 TABLET in 1 BOTTLESep 30, 2006
55111-118-244 BLISTER PACK in 1 CARTON (55111-118-24) / 6 TABLET in 1 BLISTER PACKSep 30, 2006
55111-118-301 BOTTLE in 1 CARTON (55111-118-30) / 30 TABLET in 1 BOTTLESep 30, 2006
55111-118-353 BLISTER PACK in 1 CARTON (55111-118-35) / 6 TABLET in 1 BLISTER PACKSep 30, 2006
55111-118-401 BOTTLE in 1 CARTON (55111-118-40) / 40 TABLET in 1 BOTTLEOct 1, 2020
55111-118-601 BOTTLE in 1 CARTON (55111-118-60) / 60 TABLET in 1 BOTTLESep 30, 2006
55111-118-791 BLISTER PACK in 1 CARTON (55111-118-79) / 10 TABLET in 1 BLISTER PACKSep 30, 2006
55111-118-813 BLISTER PACK in 1 CARTON (55111-118-81) / 10 TABLET in 1 BLISTER PACKSep 30, 2006
55111-118-901 BOTTLE in 1 CARTON (55111-118-90) / 90 TABLET in 1 BOTTLESep 30, 2006

Recalls mentioning this NDC

Other Famotidine products