NDC 71335-1318 – Felodipine

Felodipine 5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-1318

Product details

Brand name
Felodipine
Generic name
Felodipine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203417
Marketed since
January 17, 2013
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Felodipine →

Package NDC codes (1)

Package NDCDescriptionSince
71335-1318-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1318-1)Aug 27, 2019

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