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CARBIDOPA AND LEVODOPA

NDC 62756-517 · Sun Pharmaceutical Industries, Inc.

Generic nameCARBIDOPA AND LEVODOPA
Dosage formTABLET
RouteORAL
Active ingredient(s)CARBIDOPA, LEVODOPA
Strength10; 100 mg/1; mg/1
Pharmacologic classAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
Marketing categoryANDA

Packages

62756-517-08 — 100 TABLET in 1 BOTTLE (62756-517-08)

62756-517-13 — 500 TABLET in 1 BOTTLE (62756-517-13)

62756-517-18 — 1000 TABLET in 1 BOTTLE (62756-517-18)

62756-517-83 — 30 TABLET in 1 BOTTLE (62756-517-83)

62756-517-88 — 100 TABLET in 1 BOTTLE (62756-517-88)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62332-332 — 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, 62756-518 — CARBIDOPA AND LEVODOPA, 62756-985 — CARBIDOPA AND LEVODOPA, 63083-1514 — L-Dopa, 63629-4134 — Carbidopa and Levodopa, 63629-9154 — CARBIDOPA AND LEVODOPA, 64896-661 — Carbidopa and Levodopa, 64896-662 — Carbidopa and Levodopa, 64896-663 — Carbidopa and Levodopa, 64896-664 — Carbidopa and Levodopa, 64896-967 — 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.