NDC 50090-6182

STEGLATRO

Ertugliflozin

STEGLATRO is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Ertugliflozin Pidolate.

• Product ID: 50090-6182_62ebce91-1a76-4c3b-bc52-4953699e116c
• NDC: 50090-6182
• Product Type: Human Prescription Drug
• Proprietary Name: STEGLATRO
• Generic Name: Ertugliflozin
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2017-12-19
• Marketing Category: NDA /
• Application Number: NDA209803
• Labeler Name: A-S Medication Solutions
• Substance Name: ERTUGLIFLOZIN PIDOLATE
• Active Ingredient Strength: 5 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 50090-6182-0

90 TABLET, FILM COATED in 1 BOTTLE (50090-6182-0)

• Marketing Start Date: 2022-10-20
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "STEGLATRO" or generic name "Ertugliflozin"

NDC	Brand Name	Generic Name
0006-5363	STEGLATRO	ertugliflozin
0006-5364	STEGLATRO	ertugliflozin
50090-6182	STEGLATRO	ertugliflozin
50090-6183	STEGLATRO	ertugliflozin