NDC 62756-518 – Carbidopa And Levodopa

Carbidopa 25 mg/1; Levodopa 100 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC62756-518

Product details

Brand name
Carbidopa And Levodopa
Generic name
Carbidopa And Levodopa
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078536
Marketed since
October 28, 2008
Listing expires
December 31, 2026
Pharmacologic class
Aromatic Amino Acid

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
62756-518-08100 TABLET in 1 BOTTLE (62756-518-08)Oct 28, 2008
62756-518-13500 TABLET in 1 BOTTLE (62756-518-13)Oct 28, 2008
62756-518-181000 TABLET in 1 BOTTLE (62756-518-18)Oct 28, 2008
62756-518-8330 TABLET in 1 BOTTLE (62756-518-83)Oct 28, 2008
62756-518-88100 TABLET in 1 BOTTLE (62756-518-88)Oct 28, 2008

Recalls mentioning this NDC

Other Carbidopa and Levodopa products