What is NDC 27241-294?

27241-294 is the product NDC for Prucalopride, Prucalopride 1 mg/1 tablet, listed with the FDA by Ajanta Pharma USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Ajanta Pharma USA Inc., NDC labeler code 27241. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Prucalopride?

33 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Prucalopride NDC 27241-294 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)27241-294Labeler and product segments. Claims need a package NDC.

Product NDC at billing width27241-0294Add 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
27241-294-30	2724102943027241029430	30 TABLET in 1 BOTTLE (27241-294-30)Marketed from Jan 16, 2026

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): Prucalopride
Generic name (nonproprietary): prucalopride
Active ingredients: Prucalopride — 1 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Ajanta Pharma USA Inc.NDC labeler code 27241
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219220
Marketing start: Jan 16, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin 4 Receptor Agonists (Mechanism)
Identifiers: Product ID 27241-294_753b960a-a820-4159-b393-96a243bc0150SPL ID 753b960a-a820-4159-b393-96a243bc0150SPL set ID c9d7152d-b117-4346-b60c-dc87b59ead09RxCUI 2107345, 2107353UNII 0A09IUW5TPUPC 0327241295300, 0327241294303
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

N427241029430 followed by a unit qualifier and the quantity

Package 27241-0294-30. 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 Mar 24, 2026.

Indications (excerpt from the label)

Prucalopride tablets are indicated for the treatment of chronic idiopathic constipation (CIC) in adults. Prucalopride tablet is a serotonin-4 (5-HT 4 ) receptor agonist indicated for the treatment of chronic idiopathic constipation (CIC) in adults. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 27241-294

What is NDC 27241-294?: 27241-294 is the product NDC for Prucalopride, Prucalopride 1 mg/1 tablet, listed with the FDA by Ajanta Pharma USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Prucalopride.
What is the active ingredient?: Prucalopride.
Who is the labeler?: Ajanta Pharma USA Inc., NDC labeler code 27241. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Prucalopride?: 33 other product NDCs are listed under this name. See all Prucalopride 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 Prucalopride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Prucalopride	Prucalopride succinate 1 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-077	46708-0077-30
Prucalopride	Prucalopride succinate 2 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-078	46708-0078-30
Prucalopride	Prucalopride succinate 1 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-077	62332-0077-30
Prucalopride	Prucalopride succinate 2 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-078	62332-0078-30
prucalopride	Prucalopride succinate 1 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1899	70771-1899-03
prucalopride	Prucalopride succinate 2 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1900	70771-1900-03
prucalopride	Prucalopride succinate 1 mg/1	Tablet, Film coatedOral	Viona Pharmaceuticals Inc	72578-221	72578-0221-06
prucalopride	Prucalopride succinate 2 mg/1	Tablet, Film coatedOral	Viona Pharmaceuticals Inc	72578-222	72578-0222-06
Prucalopride	Prucalopride 2 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-295	27241-0295-30
Prucalopride	Prucalopride succinate 1 mg/1	Tablet, Film coatedOral	AvKARE	73190-038	73190-0038-30

All 34 Prucalopride NDCs

Other NDCs under ANDA 219220

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

FDA NDC Directory listings under ANDA 219220
Product	Strength	Form · route	Labeler	Product NDC
Prucalopride	Prucalopride 2 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-295