NDC 67877-708 – Sacubitril and Valsartan

Sacubitril 49 mg/1; Valsartan 51 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC67877-708

Product details

Brand name
Sacubitril and Valsartan
Generic name
Sacubitril and Valsartan
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213764
Marketed since
July 23, 2025
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Neprilysin Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sacubitril and Valsartan →

Package NDC codes (2)

Package NDCDescriptionSince
67877-708-51180 TABLET, FILM COATED in 1 BOTTLE (67877-708-51)Jul 23, 2025
67877-708-6060 TABLET, FILM COATED in 1 BOTTLE (67877-708-60)Jul 23, 2025

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