United States · FDA National Drug Code directory

Carbidopa-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
72888-107_519a6595-11b5-ab1c-e063-6394a90a0223
Product NDC
72888-107
Form
TABLET
Composition / generic term
carbidopa and levodopa
Labeler
Advagen Pharma Ltd.,
Marketing category
ANDA
Marketing start / end (source format)
20220921
Source listing expiry
20271231

Source-listed ingredients

  • CARBIDOPA — 25 mg/1
  • LEVODOPA — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (72888-107-00) · 72888-107-00
  • 100 TABLET in 1 BOTTLE (72888-107-01) · 72888-107-01
  • 500 TABLET in 1 BOTTLE (72888-107-05) · 72888-107-05
  • 30 TABLET in 1 BOTTLE (72888-107-30) · 72888-107-30

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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