What is NDC 62756-518?

62756-518 is the product NDC for Carbidopa And Levodopa, Carbidopa 25 mg/1; Levodopa 100 mg/1 tablet, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 62756. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Carbidopa And Levodopa?

97 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Carbidopa And Levodopa NDC 62756-518

NDC codes

FDA NDC Directory

Product NDC (as listed)62756-518Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62756-0518Add 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
62756-518-08	6275605180862756051808	100 TABLET in 1 BOTTLE (62756-518-08)Marketed from Oct 28, 2008
62756-518-13	6275605181362756051813	500 TABLET in 1 BOTTLE (62756-518-13)Marketed from Oct 28, 2008
62756-518-18	6275605181862756051818	1000 TABLET in 1 BOTTLE (62756-518-18)Marketed from Oct 28, 2008
62756-518-83	6275605188362756051883	30 TABLET in 1 BOTTLE (62756-518-83)Marketed from Oct 28, 2008
62756-518-88	6275605188862756051888	100 TABLET in 1 BOTTLE (62756-518-88)Marketed from Oct 28, 2008

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
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 62756
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078536
Marketing start: Oct 28, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Aromatic (Chemical structure)
Identifiers: Product ID 62756-518_d77ed25a-588d-4d22-855f-f93ba5b4003cSPL ID d77ed25a-588d-4d22-855f-f93ba5b4003cSPL set ID 829c35f9-ace0-11dd-8800-f3e252b43544RxCUI 197443, 197444, 197445UNII MNX7R8C5VO, 46627O600JUPC 0362756517882, 0362756519886, 0362756518889
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

N462756051808 followed by a unit qualifier and the quantity

Package 62756-0518-08. 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 Aug 13, 2021.

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, USP. 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. …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62756-518

What is NDC 62756-518?: 62756-518 is the product NDC for Carbidopa And Levodopa, Carbidopa 25 mg/1; Levodopa 100 mg/1 tablet, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Carbidopa And Levodopa.
What is the active ingredient?: Carbidopa, Levodopa.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 62756. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Carbidopa And Levodopa?: 97 other product NDCs are listed under this name. See all Carbidopa And Levodopa NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Carbidopa And Levodopa NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Carbidopa and Levodopa	Carbidopa 25 mg/1; Levodopa 250 mg/1	TabletOral	Coupler LLC	67046-1689	67046-1689-03
Carbidopa and Levodopa	Carbidopa 25 mg/1; Levodopa 100 mg/1	TabletOral	AvPAK	50268-202	50268-0202-15
Carbidopa and Levodopa	Carbidopa 48.75 mg/1; Levodopa 195 mg/1	Capsule, Extended releaseOral	REMEDYREPACK INC.	70518-4621	70518-4621-00
Carbidopa and Levodopa	Carbidopa 23.75 mg/1; Levodopa 95 mg/1	Capsule, Extended releaseOral	REMEDYREPACK INC.	70518-4618	70518-4618-00
Carbidopa and Levodopa	Carbidopa 25 mg/1; Levodopa 250 mg/1	TabletOral	REMEDYREPACK INC.	70518-4620	70518-4620-00
Carbidopa and Levodopa	Carbidopa 36.25 mg/1; Levodopa 145 mg/1	Capsule, Extended releaseOral	REMEDYREPACK INC.	70518-4630	70518-4630-00
Carbidopa and Levodopa	Carbidopa 61.25 mg/1; Levodopa 245 mg/1	Capsule, Extended releaseOral	REMEDYREPACK INC.	70518-4610	70518-4610-00
Carbidopa And Levodopa	Carbidopa 25 mg/1; Levodopa 250 mg/1	TabletOral	Coupler LLC	67046-1668	67046-1668-03
Carbidopa and Levodopa	Carbidopa hydrate 25 mg/1; Levodopa 100 mg/1	Tablet, Extended releaseOral	Safecor Health, LLC	48433-015	48433-0015-20
Carbidopa and Levodopa	Carbidopa hydrate 50 mg/1; Levodopa 200 mg/1	Tablet, Extended releaseOral	Safecor Health, LLC	48433-016	48433-0016-20

All 98 Carbidopa And Levodopa NDCs

Other NDCs under ANDA 078536

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

FDA NDC Directory listings under ANDA 078536
Product	Strength	Form · route	Labeler	Product NDC
Carbidopa And Levodopa	Carbidopa 10 mg/1; Levodopa 100 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	62756-517
Carbidopa And Levodopa	Carbidopa 25 mg/1; Levodopa 250 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	62756-985
Carbidopa And Levodopa	Carbidopa 25 mg/1; Levodopa 250 mg/1	TabletOral	Bryant Ranch Prepack	63629-9154
Carbidopa And Levodopa	Carbidopa 25 mg/1; Levodopa 100 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-2240