NDC 68462-320 – Ranolazine

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

Human Prescription Drug 2 recalls

Product NDC68462-320

Product details

Brand name
Ranolazine
Generic name
Ranolazine
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211082
Marketed since
July 5, 2019
Listing expires
December 31, 2027
Pharmacologic class
Anti-anginal

Active ingredients

Uses, dosage, side effects and warnings for Ranolazine →

Package NDC codes (2)

Package NDCDescriptionSince
68462-320-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-320-05)Jul 5, 2019
68462-320-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-320-60)Jul 5, 2019

Recalls mentioning this NDC

Other Ranolazine products