NDC 53746-253 – Ranitidine

Ranitidine Hydrochloride 150 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC53746-253

Product details

Brand name
Ranitidine
Generic name
Ranitidine
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077824
Marketed since
December 16, 2009
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ranitidine →

Package NDC codes (5)

Package NDCDescriptionSince
53746-253-01100 TABLET in 1 BOTTLE (53746-253-01)Dec 16, 2009
53746-253-05500 TABLET in 1 BOTTLE (53746-253-05)Dec 16, 2009
53746-253-101000 TABLET in 1 BOTTLE (53746-253-10)Dec 16, 2009
53746-253-18180 TABLET in 1 BOTTLE (53746-253-18)Dec 16, 2009
53746-253-6060 TABLET in 1 BOTTLE (53746-253-60)Dec 16, 2009

Recalls mentioning this NDC

Other Ranitidine products