NDC 0006-5363 – Steglatro

Ertugliflozin Pidolate 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC0006-5363

Product details

Brand name
Steglatro
Generic name
Ertugliflozin
Labeler
Merck Sharp & Dohme LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA209803
Marketed since
December 19, 2017
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Steglatro →

Package NDC codes (5)

Package NDCDescriptionSince
0006-5363-0330 TABLET, FILM COATED in 1 BOTTLE (0006-5363-03)Dec 19, 2017
0006-5363-0690 TABLET, FILM COATED in 1 BOTTLE (0006-5363-06)Dec 19, 2017
0006-5363-07500 TABLET, FILM COATED in 1 BOTTLE (0006-5363-07)Dec 19, 2017
0006-5363-092 BOTTLE in 1 CARTON (0006-5363-09) / 7 TABLET, FILM COATED in 1 BOTTLE (0006-5363-08)Dec 19, 2017
0006-5363-1030 TABLET, FILM COATED in 1 BOTTLE (0006-5363-10)Dec 19, 2017

Recalls mentioning this NDC

Other Steglatro products