NDC 0904-6822 – Entacapone

Entacapone 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC0904-6822

Product details

Brand name
Entacapone
Generic name
Entacapone
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203437
Marketed since
June 19, 2015
Listing expires
December 31, 2026
Pharmacologic class
Catechol-O-Methyltransferase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Entacapone →

Package NDC codes (1)

Package NDCDescriptionSince
0904-6822-0730 BLISTER PACK in 1 CARTON (0904-6822-07) / 1 TABLET, FILM COATED in 1 BLISTER PACKMay 2, 2024

Recalls mentioning this NDC

Other Entacapone products