NDC 65862-675 – Felodipine

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

Human Prescription Drug

Product NDC65862-675

Product details

Brand name
Felodipine
Generic name
Felodipine
Labeler
Aurobindo Pharma Limited
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 (4)

Package NDCDescriptionSince
65862-675-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-675-01)Jan 17, 2013
65862-675-7810 BLISTER PACK in 1 CARTON (65862-675-78) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-675-10)Jan 17, 2013
65862-675-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-675-90)Jan 17, 2013
65862-675-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-675-99)Jan 17, 2013

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