NDC 23155-050 – Felodipine

Felodipine 10 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 1 recall

Product NDC23155-050

Product details

Brand name
Felodipine
Generic name
Felodipine
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA201964
Marketed since
November 8, 2013
Listing expires
December 31, 2027
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Felodipine →

Package NDC codes (1)

Package NDCDescriptionSince
23155-050-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-050-01)Nov 8, 2013

Recalls mentioning this NDC

Other Felodipine products