NDC 71205-922 – Felodipine

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

Human Prescription Drug

Product NDC71205-922

Product details

Brand name
Felodipine
Generic name
Felodipine
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204800
Marketed since
October 12, 2020
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Felodipine →

Package NDC codes (6)

Package NDCDescriptionSince
71205-922-00100 TABLET, FILM COATED in 1 BOTTLE (71205-922-00)Jun 18, 2021
71205-922-3030 TABLET, FILM COATED in 1 BOTTLE (71205-922-30)Jun 18, 2021
71205-922-55500 TABLET, FILM COATED in 1 BOTTLE (71205-922-55)Jun 18, 2021
71205-922-6060 TABLET, FILM COATED in 1 BOTTLE (71205-922-60)Jun 18, 2021
71205-922-72120 TABLET, FILM COATED in 1 BOTTLE (71205-922-72)Jun 18, 2021
71205-922-9090 TABLET, FILM COATED in 1 BOTTLE (71205-922-90)Jun 18, 2021

Other Felodipine products