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Carbidopa and Levodopa

NDC 62332-332 · Alembic Pharmaceuticals Inc.

Generic nameCarbidopa and Levodopa
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)CARBIDOPA, LEVODOPA
Strength25; 100 mg/1; mg/1
Pharmacologic classAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
Marketing categoryANDA

Packages

62332-332-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-332-30)

62332-332-31 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-332-31)

62332-332-91 — 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-332-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-0192 — Carbidopa and Levodopa, 55154-2643 — Carbidopa and Levodopa, 59651-146 — Carbidopa, 59651-456 — Carbidopa and Levodopa, 59651-457 — Carbidopa and Levodopa, 59651-458 — Carbidopa and Levodopa, 60219-2033 — CARBIDOPA and LEVODOPA, 60219-2034 — CARBIDOPA and LEVODOPA, 60687-661 — Carbidopa and Levodopa, 60687-836 — Carbidopa and Levodopa, 62332-333 — Carbidopa and Levodopa, 62332-795 — carbidopa, levodopa and entacapone, 62332-796 — carbidopa, levodopa and entacapone, 62332-797 — carbidopa, levodopa and entacapone, 62332-798 — carbidopa, levodopa and entacapone, 62332-799 — carbidopa, levodopa and entacapone, 62332-800 — carbidopa, levodopa and entacapone, 62756-457 — CARBIDOPA AND LEVODOPA, 62756-461 — CARBIDOPA AND LEVODOPA, 62756-517 — CARBIDOPA AND LEVODOPA, +147 more

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