NDC 71205-867 – Ranolazine

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

Human Prescription Drug

Product NDC71205-867

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211829
Marketed since
August 24, 2021
Listing expires
December 31, 2026
Pharmacologic class
Anti-anginal

Active ingredients

Uses, dosage, side effects and warnings for Ranolazine →

Package NDC codes (7)

Package NDCDescriptionSince
71205-867-00100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-00)Dec 17, 2021
71205-867-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-30)Dec 17, 2021
71205-867-55500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-55)Dec 17, 2021
71205-867-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-60)Dec 17, 2021
71205-867-72120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-72)Dec 17, 2021
71205-867-78180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-78)Dec 17, 2021
71205-867-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-867-90)Dec 17, 2021

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