Carbidopa And Levodopa NDC 62756-461

NDC codes

FDA NDC Directory

Product NDC (as listed)62756-461Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62756-0461Add 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
62756-461-08	62756046108	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-08)Marketed from Aug 23, 2007
62756-461-18	62756046118	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-18)Marketed from Aug 23, 2007
62756-461-83	62756046183	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-83)Marketed from Aug 23, 2007

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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, Extended release
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077828
Marketing start: Aug 23, 2007
Listing expires: Dec 31, 2027
Other FDA classes: Aromatic (Chemical structure)
Identifiers: Product ID 62756-461_536b1b5e-fcd0-4563-e063-6294a90a182eSPL ID 536b1b5e-fcd0-4563-e063-6294a90a182eSPL set ID d2a64f14-f638-49d9-8a96-cb7ae46ac3eaRxCUI 308988, 308989UNII 46627O600J, MNX7R8C5VOUPC 0362756457836
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

N462756046108 followed by a unit qualifier and the quantity

Package 62756-0461-08. 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 Jun 4, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carbidopa and levodopa extended-release tablets are indicated in the treatment of Parkinson's disease, post-encephalitic parkinsonism, and symptomatic parkinsonism that may follow carbon monoxide intoxication or manganese intoxication.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077828

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

FDA NDC Directory listings under ANDA 077828
Product	Strength	Form · route	Labeler	Product NDC
Carbidopa And Levodopa	Carbidopa 50 mg/1; Levodopa 200 mg/1	Tablet, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	62756-457