Carbidopa and Levodopa Tablets

Manufacturer
Zydus Lifesciences Limited
Effective date
2024-11-26
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:48:32

Label at a glance#

ProductCarbidopa and Levodopa
Active ingredientCARBIDOPA, LEVODOPA
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70771-1694-1

Carbidopa and Levodopa Tablets, USP 10 mg/100 mg

100 Tablets

Rx only

10 mg/100 mg label
10 mg/100 mg label

NDC 70771-1695-1

Carbidopa and Levodopa Tablets, USP 25 mg/100 mg

100 Tablets

Rx only

25 mg/100 mg label
25 mg/100 mg label

NDC 70771-1696-1

Carbidopa and Levodopa Tablets, USP 25 mg/250 mg

100 Tablets

Rx only

25 mg/250 mg label
25 mg/250 mg label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
7c77eebd-71e0-4fdd-a51a-3c0742f599a654c08e94-c97b-4717-adfc-ea12083dbb412024-11-26Exact identifier
spl id: 7c77eebd-71e0-4fdd-a51a-3c0742f599a6
spl set id: 54c08e94-c97b-4717-adfc-ea12083dbb41

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.