NDC 46708-557 – sacubitril and valsartan

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

Human Prescription Drug

Product NDC46708-557

Product details

Brand name
sacubitril and valsartan
Generic name
sacubitril and valsartan
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213682
Marketed since
November 4, 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 (4)

Package NDCDescriptionSince
46708-557-10100 BLISTER PACK in 1 CARTON (46708-557-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKNov 4, 2024
46708-557-45180 TABLET, FILM COATED in 1 BOTTLE (46708-557-45)Nov 4, 2024
46708-557-6060 TABLET, FILM COATED in 1 BOTTLE (46708-557-60)Nov 4, 2024
46708-557-911000 TABLET, FILM COATED in 1 BOTTLE (46708-557-91)Nov 4, 2024

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