United States · FDA National Drug Code directory
Carbidopa and Levodopa
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 60219-2034_b5ad7e75-c6cd-4b2d-a3bf-e2e860d5b9c1
- Product NDC
- 60219-2034
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- CARBIDOPA and LEVODOPA
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221221
- Source listing expiry
- 20271231
Source-listed ingredients
- CARBIDOPA HYDRATE — 50 mg/1
- LEVODOPA — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60219-2034-1) · 60219-2034-1
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (60219-2034-3) · 60219-2034-3
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60219-2034-5) · 60219-2034-5
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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