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
- 0093-9703_f9b97c07-d9fd-456d-ac85-4b41cd95149e
- Product NDC
- 0093-9703
- Form
- TABLET
- Composition / generic term
- Carbidopa and levodopa
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231215
- Source listing expiry
- 20271231
Source-listed ingredients
- CARBIDOPA HYDRATE — 25 mg/1
- LEVODOPA — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0093-9703-01) · 0093-9703-01
- 500 TABLET in 1 BOTTLE (0093-9703-05) · 0093-9703-05
- 1000 TABLET in 1 BOTTLE (0093-9703-10) · 0093-9703-10
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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