NDC 68682-938 – Tolcapone

Tolcapone 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68682-938

Product details

Brand name
Tolcapone
Generic name
Tolcapone
Labeler
Oceanside Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA020697
Marketed since
July 27, 2004
Listing expires
December 31, 2026
Pharmacologic class
Catechol-O-Methyltransferase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tolcapone →

Package NDC codes (1)

Package NDCDescriptionSince
68682-938-9090 TABLET, FILM COATED in 1 BOTTLE (68682-938-90)Jul 27, 2004

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