ropinirole hydrochloride NDC 71335-1434

Product information

Brand name (proprietary)

ropinirole hydrochloride

Generic name (nonproprietary)

ropinirole hydrochloride

Active ingredients

Ropinirole hydrochloride — 1 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 078110

Marketing start

Sep 20, 2011

Listing expires

Dec 31, 2026

Other FDA classes

Dopamine Agonists (Mechanism)

Identifiers

Product ID 71335-1434_d88b1f49-8ea3-43fa-ae34-0cb10ca3a562SPL ID d88b1f49-8ea3-43fa-ae34-0cb10ca3a562SPL set ID 6c10444a-48da-469d-bf8f-1e6e0b7e15f8RxCUI 312845, 312847, 314208UNII D7ZD41RZI9

Pharmacologic class

Nonergot Dopamine 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

N471335143401 followed by a unit qualifier and the quantity Copy

Package 71335-1434-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 078110

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

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