NDC 0603-3583 – Felodipine

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

Human Prescription Drug

Product NDC0603-3583

Product details

Brand name
Felodipine
Generic name
Felodipine
Labeler
Endo USA, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA200815
Marketed since
December 15, 2011
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Felodipine →

Package NDC codes (2)

Package NDCDescriptionSince
0603-3583-21100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3583-21)Dec 15, 2011
0603-3583-28500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3583-28)Dec 15, 2011

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