Carbidopa (carbidopa tablets) NDC 68682-200

NDC codes

FDA NDC Directory

Product NDC (as listed)68682-200Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68682-0200Add 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	Copy
68682-200-25	68682020025	100 TABLET in 1 BOTTLE (68682-200-25)Marketed from Apr 4, 2014

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
Generic name (nonproprietary): carbidopa tablets
Active ingredients: Carbidopa — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Oceanside Pharmaceuticals
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 017830
Marketing start: Apr 4, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 68682-200_ccf10efe-4fda-40a4-8f20-1ccefb151a15SPL ID ccf10efe-4fda-40a4-8f20-1ccefb151a15SPL set ID d5204e5e-10ef-4758-8fc6-cb710048c687RxCUI 260260UNII MNX7R8C5VO

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

N468682020025 followed by a unit qualifier and the quantity

Package 68682-0200-25. 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

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