NDC 70625-207 – Ranolazine

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

Human Prescription Drug

Product NDC70625-207

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
SunGen Pharma LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212781
Marketed since
April 1, 2020
Listing expires
December 31, 2027
Pharmacologic class
Anti-anginal

Active ingredients

Uses, dosage, side effects and warnings for Ranolazine →

Package NDC codes (3)

Package NDCDescriptionSince
70625-207-0014563 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOX (70625-207-00)Apr 1, 2020
70625-207-0160 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70625-207-01)Apr 1, 2020
70625-207-02500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70625-207-02)Apr 1, 2020

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