NDC 71205-878 – Carbidopa and Levodopa

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

Human Prescription Drug

Product NDC71205-878

Product details

Brand name
Carbidopa and Levodopa
Generic name
Carbidopa and Levodopa
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214092
Marketed since
September 30, 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 (9)

Package NDCDescriptionSince
71205-878-00100 TABLET in 1 BOTTLE, PLASTIC (71205-878-00)Nov 5, 2021
71205-878-111000 TABLET in 1 BOTTLE, PLASTIC (71205-878-11)Nov 5, 2021
71205-878-3030 TABLET in 1 BOTTLE, PLASTIC (71205-878-30)Nov 5, 2021
71205-878-55500 TABLET in 1 BOTTLE, PLASTIC (71205-878-55)Nov 5, 2021
71205-878-6060 TABLET in 1 BOTTLE, PLASTIC (71205-878-60)Nov 5, 2021
71205-878-64240 TABLET in 1 BOTTLE, PLASTIC (71205-878-64)Nov 5, 2021
71205-878-72120 TABLET in 1 BOTTLE, PLASTIC (71205-878-72)Nov 5, 2021
71205-878-78180 TABLET in 1 BOTTLE, PLASTIC (71205-878-78)Nov 5, 2021
71205-878-9090 TABLET in 1 BOTTLE, PLASTIC (71205-878-90)Nov 5, 2021

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