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CARBIDOPA AND LEVODOPA

NDC 47335-187 · Sun Pharmaceutical Industries, Inc.

Generic nameCARBIDOPA AND LEVODOPA
Dosage formTABLET, ORALLY DISINTEGRATING
RouteORAL
Active ingredient(s)CARBIDOPA, LEVODOPA
Strength25; 100 mg/1; mg/1
Pharmacologic classAmino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
Marketing categoryANDA

Packages

47335-187-08 — 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-187-08)

47335-187-18 — 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-187-18)

47335-187-83 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-187-83)

47335-187-88 — 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (47335-187-88)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

44911-0035 — L-Dopa, 46708-332 — Carbidopa and Levodopa, 46708-333 — Carbidopa and Levodopa, 46708-795 — carbidopa, levodopa and entacapone, 46708-796 — carbidopa, levodopa and entacapone, 46708-797 — carbidopa, levodopa and entacapone, 46708-798 — carbidopa, levodopa and entacapone, 46708-799 — carbidopa, levodopa and entacapone, 46708-800 — carbidopa, levodopa and entacapone, 47335-186 — CARBIDOPA AND LEVODOPA, 47335-188 — CARBIDOPA AND LEVODOPA, 48433-015 — carbidopa and levodopa, 48433-016 — carbidopa and levodopa, 50090-5969 — Carbidopa and Levodopa, 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, +147 more

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