NDC 42385-931 – Sacubitril and Valsartan

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

Human Prescription Drug

Product NDC42385-931

Product details

Brand name
Sacubitril and Valsartan
Generic name
Sacubitril and Valsartan
Labeler
Laurus Labs Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213676
Marketed since
November 11, 2024
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 (5)

Package NDCDescriptionSince
42385-931-18180 TABLET, FILM COATED in 1 BOTTLE (42385-931-18)Nov 11, 2024
42385-931-3030 TABLET, FILM COATED in 1 BOTTLE (42385-931-30)Nov 11, 2024
42385-931-6060 TABLET, FILM COATED in 1 BOTTLE (42385-931-60)Nov 11, 2024
42385-931-68100 BLISTER PACK in 1 CARTON (42385-931-68) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42385-931-10)Nov 11, 2024
42385-931-72100 BLISTER PACK in 1 CARTON (42385-931-72) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42385-931-17)Nov 11, 2024

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