NDC 0006-5029

VERQUVO

Vericiguat

VERQUVO is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Merck Sharp & Dohme Corp.. The primary component is Vericiguat.

• Product ID: 0006-5029_15049ae3-29b9-496a-bf12-350978af10bb
• NDC: 0006-5029
• Product Type: Human Prescription Drug
• Proprietary Name: VERQUVO
• Generic Name: Vericiguat
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2021-02-01
• Marketing Category: NDA / NDA
• Application Number: NDA214377
• Labeler Name: Merck Sharp & Dohme Corp.
• Substance Name: VERICIGUAT
• Active Ingredient Strength: 5 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 0006-5029-01

14 TABLET, FILM COATED in 1 BOTTLE (0006-5029-01)

• Marketing Start Date: 2021-02-01
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "VERQUVO" or generic name "Vericiguat"

NDC	Brand Name	Generic Name
0006-5028	VERQUVO	vericiguat
0006-5029	VERQUVO	vericiguat
0006-5030	VERQUVO	vericiguat