NDC 60687-836 – Carbidopa and Levodopa

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

Human Prescription Drug

Product NDC60687-836

Product details

Brand name
Carbidopa and Levodopa
Generic name
Carbidopa and Levodopa
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074260
Marketed since
March 16, 2024
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 (1)

Package NDCDescriptionSince
60687-836-01100 BLISTER PACK in 1 CARTON (60687-836-01) / 1 TABLET in 1 BLISTER PACK (60687-836-11)Mar 16, 2024

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