NDC 55111-396 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Otc Drug 1 recall

Product NDC55111-396

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 (10)

Package NDCDescriptionSince
55111-396-011 BOTTLE in 1 CARTON (55111-396-01) / 100 TABLET in 1 BOTTLESep 30, 2006
55111-396-081 BLISTER PACK in 1 CARTON (55111-396-08) / 8 TABLET in 1 BLISTER PACKSep 30, 2006
55111-396-131 BOTTLE in 1 CARTON (55111-396-13) / 130 TABLET in 1 BOTTLEOct 1, 2020
55111-396-165 BLISTER PACK in 1 CARTON (55111-396-16) / 5 TABLET in 1 BLISTER PACKSep 30, 2006
55111-396-321 BOTTLE in 1 CARTON (55111-396-32) / 170 TABLET in 1 BOTTLESep 30, 2006
55111-396-351 BOTTLE in 1 CARTON (55111-396-35) / 25 TABLET in 1 BOTTLESep 30, 2006
55111-396-442 BOTTLE in 1 CARTON (55111-396-44) / 100 TABLET in 1 BOTTLESep 30, 2006
55111-396-501 BOTTLE in 1 CARTON (55111-396-50) / 50 TABLET in 1 BOTTLESep 30, 2006
55111-396-651 BOTTLE in 1 CARTON (55111-396-65) / 65 TABLET in 1 BOTTLEOct 1, 2020
55111-396-901 BOTTLE in 1 CARTON (55111-396-90) / 90 TABLET in 1 BOTTLEOct 7, 2021

Recalls mentioning this NDC

Other Famotidine products