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Carbidopa and Levodopa

NDC 50228-461 · ScieGen Pharmaceuticals Inc

Generic nameCarbidopa and Levodopa
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)CARBIDOPA, LEVODOPA
Strength50; 200 mg/1; mg/1
Pharmacologic classAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
Marketing categoryANDA

Packages

50228-461-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50228-461-01)

50228-461-10 — 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (50228-461-10)

50228-461-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50228-461-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6580 — Carbidopa and Levodopa, 50090-6725 — Carbidopa and Levodopa, 50090-6727 — Carbidopa and levodopa, 50090-7186 — Carbidopa and Levodopa, 50090-7498 — Carbidopa and Levodopa, 50090-7499 — Carbidopa and Levodopa, 50228-457 — Carbidopa and Levodopa, 50228-458 — Carbidopa and Levodopa, 50228-459 — Carbidopa and Levodopa, 50228-460 — Carbidopa and Levodopa, 50268-202 — Carbidopa and Levodopa, 51079-923 — carbidopa and levodopa, 51079-978 — carbidopa and levodopa, 52817-390 — carbidopa and levodopa, 52817-391 — carbidopa and levodopa, 52817-392 — carbidopa and levodopa, 53401-020 — Carbidopa and Levodopa, 55154-0192 — Carbidopa and Levodopa, 55154-2643 — Carbidopa and Levodopa, 59651-146 — Carbidopa, +147 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.