NDC 68462-235 – Felodipine

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

Human Prescription Drug

Product NDC68462-235

Product details

Brand name
Felodipine
Generic name
Felodipine
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090365
Marketed since
December 20, 2010
Listing expires
December 31, 2027
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Felodipine →

Package NDC codes (4)

Package NDCDescriptionSince
68462-235-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-235-01)Dec 20, 2010
68462-235-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-235-10)Dec 20, 2010
68462-235-1110 BLISTER PACK in 1 CARTON (68462-235-11) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKDec 20, 2010
68462-235-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-235-90)Dec 20, 2010

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