Carbidopa and Levodopa NDC 0615-8536

NDC codes

FDA NDC Directory

Product NDC (as listed)0615-8536Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00615-8536Add 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 NDC	11-digit (billing)	Package
0615-8536-05	00615853605	15 TABLET in 1 BLISTER PACK (0615-8536-05)Marketed from Sep 10, 2024
0615-8536-28	00615853628	28 TABLET in 1 BLISTER PACK (0615-8536-28)Marketed from Sep 10, 2024
0615-8536-39	00615853639	30 TABLET in 1 BLISTER PACK (0615-8536-39)Marketed from Sep 10, 2024

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 25 mg/1Levodopa — 100 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 073589
Marketing start: May 1, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Aromatic (Chemical structure)
Identifiers: Product ID 0615-8536_4bccc4b9-7399-4dd4-9146-c5b2714f299fSPL ID 4bccc4b9-7399-4dd4-9146-c5b2714f299fSPL set ID 45909de3-0852-4e61-8a9e-23f8fcc2463aRxCUI 197443, 197444, 197445UNII 46627O600J, MNX7R8C5VO
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

N400615853605 followed by a unit qualifier and the quantity

Package 00615-8536-05. 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

Current FDA label (SPL), effective Dec 6, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carbidopa and levodopa tablets, USP are indicated in the treatment of Parkinson's disease, post-encephalitic parkinsonism, and symptomatic parkinsonism that may follow carbon monoxide intoxication or manganese intoxication. Carbidopa allows patients treated for Parkinson's disease to use much lower doses of levodopa. Some patients who responded poorly to levodopa have improved on carbidopa and levodopa tablets. This is most likely due to decreased peripheral decarboxylation of levodopa caused by administration of carbidopa rather than by a primary effect of carbidopa on the nervous system. Carbidopa has not been shown to enhance the intrinsic efficacy of levodopa. Carbi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 073589

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

FDA NDC Directory listings under ANDA 073589
Product	Strength	Form · route	Labeler	Product NDC
Carbidopa and Levodopa	Carbidopa hydrate 25 mg/1; Levodopa 100 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2643
Carbidopa and Levodopa	Carbidopa hydrate 25 mg/1; Levodopa 100 mg/1	TabletOral	Major Pharmaceuticals	0904-7501
Carbidopa and Levodopa	Carbidopa 25 mg/1; Levodopa 100 mg/1	TabletOral	Dr. Reddy's Laboratories Inc	75907-020
Carbidopa and Levodopa	Carbidopa 25 mg/1; Levodopa 100 mg/1	TabletOral	AvPAK	50268-202