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NDC 47335-0187-88

CARBIDOPA AND LEVODOPA 25 mg/1, 100 mg/1 TABLET, ORALLY DISINTEGRATING

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NDC
47335-0187-88
Generic Name
CARBIDOPA AND LEVODOPA
Brand Name
CARBIDOPA AND LEVODOPA
Strength
25 mg/1, 100 mg/1
Dosage Form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Package Size
—
Labeler
Sun Pharmaceutical Industries, Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Carbidopa and levodopa orally disintegrating tablets are indicated in the treatment of Parkinson’s disease, post-encephalitic parkinsonism, and symptomatic parkinsonism that may follow carbon monoxide intoxication or manganese intoxication. Carbidopa allows patients treated for Parkinson’s disease to use much lower doses of levodopa. Some patients who responded poorly to levodopa have improved on carbidopa and levodopa orally disintegrating tablets. This is most likely due…

Important Warnings

WARNINGS When carbidopa and levodopa orally disintegrating tablet is to be given to patients who are being treated with levodopa, levodopa must be discontinued at least twelve hours before therapy with carbidopa and levodopa orally disintegrating tablet is started. In order to reduce adverse reactions, it is necessary to individualize therapy. See DOSAGE AND ADMINISTRATION section before initiatin…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other CARBIDOPA AND LEVODOPA NDC Codes

50228-0460-0125 mg/1, 100 mg/1TABLET, EXTENDED RELEASE
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50228-0461-0150 mg/1, 200 mg/1TABLET, EXTENDED RELEASE
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62756-0517-1310 mg/1, 100 mg/1TABLET
2-Day
62756-0461-8825 mg/1, 100 mg/1TABLET, EXTENDED RELEASE
2-Day
47335-0188-8825 mg/1, 250 mg/1TABLET, ORALLY DISINTEGRATING
2-Day

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