NDC codes

FDA NDC Directory
Product NDC (as listed)67046-1614Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67046-1614Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
67046-1614-36704616140330 TABLET in 1 BLISTER PACK (67046-1614-3)Marketed from Nov 17, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Carbidopa and Levodopa
Generic name (nonproprietary)
carbidopa and levodopa
Active ingredients
Carbidopa — 10 mg/1Levodopa — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216537
Marketing start
Listing expires
Other FDA classes
Aromatic (Chemical structure)
Identifiers
Product ID 67046-1614_43ce4d9e-fb3c-ed29-e063-6294a90a99caSPL ID 43ce4d9e-fb3c-ed29-e063-6294a90a99caSPL set ID 43ce5061-0830-6f4f-e063-6394a90afc59RxCUI 197443UNII MNX7R8C5VO, 46627O600J
Pharmacologic class
Aromatic Amino Acid

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N467046161403 followed by a unit qualifier and the quantity

Package 67046-1614-03. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 216537

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 216537
ProductStrengthForm · routeLabelerProduct NDC
Carbidopa and LevodopaCarbidopa 25 mg/1; Levodopa 250 mg/1TabletOralBryant Ranch Prepack63629-4134
Carbidopa and LevodopaCarbidopa 25 mg/1; Levodopa 250 mg/1TabletOralCoupler LLC67046-1689
Carbidopa and LevodopaCarbidopa 10 mg/1; Levodopa 100 mg/1TabletOralAurobindo Pharma Limited59651-456
Carbidopa and LevodopaCarbidopa 25 mg/1; Levodopa 100 mg/1TabletOralAurobindo Pharma Limited59651-457
Carbidopa and LevodopaCarbidopa 25 mg/1; Levodopa 250 mg/1TabletOralAurobindo Pharma Limited59651-458
Carbidopa and LevodopaCarbidopa 25 mg/1; Levodopa 100 mg/1TabletOralA-S Medication Solutions50090-7498
Carbidopa and LevodopaCarbidopa 25 mg/1; Levodopa 100 mg/1TabletOralA-S Medication Solutions50090-7499
Carbidopa and LevodopaCarbidopa 25 mg/1; Levodopa 250 mg/1TabletOralREMEDYREPACK INC.70518-4620

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