NDC 63304-018 – Ranolazine

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

Human Prescription Drug

Product NDC63304-018

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211707
Marketed since
May 28, 2019
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
63304-018-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-05)May 28, 2019
63304-018-28180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-28)May 28, 2019
63304-018-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-60)May 28, 2019

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