What is NDC 70771-1355?

70771-1355 is the product NDC for Carbidopa, Carbidopa 25 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 70771. 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?

7 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Carbidopa NDC 70771-1355 | National Drug Code

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	7077113550170771135501	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 LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209910
Marketing start: Sep 6, 2018
Listing expires: Dec 31, 2027
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)

About NDC 70771-1355

What is NDC 70771-1355?: 70771-1355 is the product NDC for Carbidopa, Carbidopa 25 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Carbidopa.
What is the active ingredient?: Carbidopa.
Who is the labeler?: Zydus Lifesciences Limited, NDC labeler code 70771. 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?: 7 other product NDCs are listed under this name. See all Carbidopa 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Carbidopa	Carbidopa 25 mg/1	TabletOral	NorthStar Rx LLC	16714-067	16714-0067-01
Carbidopa	Carbidopa 25 mg/1	TabletOral	Aurobindo Pharma Limited	59651-146	59651-0146-01
Carbidopa	Carbidopa 25 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1221	70710-1221-01
Carbidopa	Carbidopa 25 mg/1	TabletOral	Novel Laboratories, Inc.	40032-980	40032-0980-0140032-0980-0340032-0980-10
Carbidopa	Carbidopa 25 mg/1	TabletOral	Lupin Pharmaceuticals,Inc.	43386-980	43386-0980-01
Carbidopa	Carbidopa 25 mg/1	TabletOral	Edenbridge Pharmaceuticals LLC.	42799-123	42799-0123-01
Carbidopacarbidopa tablets	Carbidopa 25 mg/1	TabletOral	Oceanside Pharmaceuticals	68682-200	68682-0200-25

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