NDC 67877-526 – Ranolazine

Ranolazine 1000 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC67877-526

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA209953
Marketed since
December 2, 2020
Listing expires
December 31, 2026
Pharmacologic class
Anti-anginal

Active ingredients

Uses, dosage, side effects and warnings for Ranolazine →

Package NDC codes (3)

Package NDCDescriptionSince
67877-526-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-526-05)Dec 2, 2020
67877-526-3810 BLISTER PACK in 1 CARTON (67877-526-38) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKDec 2, 2020
67877-526-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-526-60)Dec 2, 2020

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