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NDC 62756-0457-88

CARBIDOPA AND LEVODOPA 50 mg/1, 200 mg/1 TABLET, EXTENDED RELEASE

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NDC
62756-0457-88
Generic Name
CARBIDOPA AND LEVODOPA
Brand Name
CARBIDOPA AND LEVODOPA
Strength
50 mg/1, 200 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Package Size
—
Labeler
Sun Pharmaceutical Industries, Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Carbidopa and levodopa extended-release 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.

Important Warnings

WARNINGS When patients are receiving levodopa without a decarboxylase inhibitor, levodopa must be discontinued at least twelve hours before carbidopa and levodopa extended-release tablets are started. In order to reduce adverse reactions, it is necessary to individualize therapy. See DOSAGE AND ADMINISTRATION section before initiating therapy. Carbidopa and levodopa extended-release tablets should…

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
47335-0187-8825 mg/1, 100 mg/1TABLET, ORALLY DISINTEGRATING
2-Day
62756-0461-8825 mg/1, 100 mg/1TABLET, EXTENDED RELEASE
2-Day

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