NDC 55111-131 – Ranitidine

Ranitidine Hydrochloride 75 mg/1 · Tablet · Oral

Human Otc Drug 1 recall

Product NDC55111-131

Product details

Brand name
Ranitidine
Generic name
Ranitidine
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075294
Marketed since
March 1, 2000
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ranitidine →

Package NDC codes (10)

Package NDCDescriptionSince
55111-131-041 BOTTLE in 1 CARTON (55111-131-04) / 120 TABLET in 1 BOTTLEMar 1, 2000
55111-131-142 BLISTER PACK in 1 CARTON (55111-131-14) / 10 TABLET in 1 BLISTER PACKMar 1, 2000
55111-131-301 BOTTLE in 1 CARTON (55111-131-30) / 30 TABLET in 1 BOTTLEMar 1, 2000
55111-131-371 BOTTLE in 1 CARTON (55111-131-37) / 160 TABLET in 1 BOTTLEMar 1, 2000
55111-131-451 BOTTLE in 1 CARTON (55111-131-45) / 45 TABLET in 1 BOTTLEMar 1, 2000
55111-131-601 BOTTLE in 1 CARTON (55111-131-60) / 60 TABLET in 1 BOTTLEMar 1, 2000
55111-131-791 BLISTER PACK in 1 CARTON (55111-131-79) / 10 TABLET in 1 BLISTER PACKMar 1, 2000
55111-131-801 BOTTLE in 1 CARTON (55111-131-80) / 80 TABLET in 1 BOTTLEMar 1, 2000
55111-131-813 BLISTER PACK in 1 CARTON (55111-131-81) / 10 TABLET in 1 BLISTER PACKMar 1, 2000
55111-131-901 BOTTLE in 1 CARTON (55111-131-90) / 90 TABLET in 1 BOTTLEMar 1, 2000

Recalls mentioning this NDC

Other Ranitidine products