NDC 68180-354 – Ranolazine

Ranolazine 500 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC68180-354

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA201046
Marketed since
February 27, 2019
Listing expires
December 31, 2026
Pharmacologic class
Anti-anginal

Active ingredients

Uses, dosage, side effects and warnings for Ranolazine →

Package NDC codes (0)

Package NDCDescriptionSince

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