prucalopride NDC 70771-1900

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1900Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1900Add 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
70771-1900-3	70771190003	30 TABLET, FILM COATED in 1 BOTTLE (70771-1900-3)Marketed from Feb 2, 2026

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): prucalopride
Generic name (nonproprietary): prucalopride
Active ingredients: Prucalopride succinate — 2 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Zydus Lifesciences Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218056
Marketing start: Feb 2, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin 4 Receptor Agonists (Mechanism)
Identifiers: Product ID 70771-1900_051f4f7e-88e8-4706-8183-dbd3f9d42d72SPL ID 051f4f7e-88e8-4706-8183-dbd3f9d42d72SPL set ID da37395d-0a05-4fdc-ab5c-eb7caed62bf1RxCUI 2107345, 2107353UNII 4V2G75E1CK
Pharmacologic class: Serotonin-4 Receptor Agonist

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

N470771190003 followed by a unit qualifier and the quantity

Package 70771-1900-03. 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 Jan 30, 2026.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 218056

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

FDA NDC Directory listings under ANDA 218056
Product	Strength	Form · route	Labeler	Product NDC
prucalopride	Prucalopride succinate 1 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1899
prucalopride	Prucalopride succinate 1 mg/1	Tablet, Film coatedOral	Viona Pharmaceuticals Inc	72578-221
prucalopride	Prucalopride succinate 2 mg/1	Tablet, Film coatedOral	Viona Pharmaceuticals Inc	72578-222