NDC 62756-985 – Carbidopa And Levodopa

Carbidopa 25 mg/1; Levodopa 250 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC62756-985

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
August 12, 2021
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 (2)

Package NDCDescriptionSince
62756-985-01100 TABLET in 1 BOTTLE (62756-985-01)Aug 12, 2021
62756-985-02500 TABLET in 1 BOTTLE (62756-985-02)Aug 12, 2021

Recalls mentioning this NDC

Other Carbidopa and Levodopa products