Carbidopa NDC 70771-1355

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1355Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1355Add 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
70771-1355-1	70771135501	100 TABLET in 1 BOTTLE (70771-1355-1)Marketed from Sep 6, 2018

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Active ingredients: Carbidopa — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Lifesciences Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209910
Marketing start: Sep 6, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 70771-1355_46adf313-2cc6-42be-ab34-627223b59ad6SPL ID 46adf313-2cc6-42be-ab34-627223b59ad6SPL set ID 83012ccc-aba2-45bb-9326-dc30cdeb4e3bRxCUI 260260UNII MNX7R8C5VOUPC 0370710122119

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

N470771135501 followed by a unit qualifier and the quantity

Package 70771-1355-01. 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 Nov 26, 2024.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209910

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

FDA NDC Directory listings under ANDA 209910
Product	Strength	Form · route	Labeler	Product NDC
Carbidopa	Carbidopa 25 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1221