NDC 16571-693 – Carbidopa, Levodopa And Entacapone

Carbidopa 37.5 mg/1; Levodopa 150 mg/1; Entacapone 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC16571-693

Product details

Brand name
Carbidopa, Levodopa And Entacapone
Generic name
Carbidopa, Levodopa And Entacapone
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213212
Marketed since
August 5, 2021
Listing expires
December 31, 2027
Pharmacologic class
Aromatic Amino Acid; Catechol-O-Methyltransferase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Carbidopa, Levodopa, and Entacapone →

Package NDC codes (1)

Package NDCDescriptionSince
16571-693-01100 TABLET, FILM COATED in 1 BOTTLE (16571-693-01)Aug 5, 2021

Recalls mentioning this NDC

Other Carbidopa, Levodopa, and Entacapone products