Carbidopa And Levodopa Capsule, Extended Release
NDC Package 70518-4621-0
Package Information
Carbidopa And Levodopa capsules is carbidopa and levodopa extended-release capsules are indicated for the treatment of Parkinson's disease, post-encephalitic parkinsonism, and parkinsonism that may follow carbon monoxide intoxication or manganese intoxication. This formulation utilizes a capsule, extended release delivery system. Marketed by Remedyrepack Inc., this product is identified by NDC 70518-4621 and is authorized under FDA application NDA203312.
Identification & Billing
- RxCUI: 1600914 - carbidopa 48.75 MG / levodopa 195 MG 8HR Extended Release Oral Capsule
- RxCUI: 1600914 - 8 HR carbidopa 48.75 MG / levodopa 195 MG Extended Release Oral Capsule
- RxCUI: 1600914 - 8 HR Carbidopa 48.75 MG / L-DOPA 195 MG Extended Release Oral Capsule
- RxCUI: 1600914 - carbidopa 48.75 MG / levodopa 195 MG 8 HR Extended Release Oral Capsule
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 70518 - Remedyrepack Inc.
- 70518-4621 - Carbidopa And Levodopa
- 70518-4621-0 - 50 POUCH in 1 BOX / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-4621-1)
- 70518-4621 - Carbidopa And Levodopa
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 70518-4621-0 identifies a specific commercial package of 50 pouch in 1 box / 1 capsule, extended release in 1 pouch (70518-4621-1) of Carbidopa And Levodopa, a human prescription drug labeled by Remedyrepack Inc.. This capsule, extended release is formulated for oral use and contains carbidopa; levodopa as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Remedyrepack Inc. on April 24, 2026. The current certification is valid through December 31, 2027.
How is this Remedyrepack Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 70518462100. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.