Prescription drug · ANDA
Ropinirole NDC 72189-364
Ropinirole hydrochloride .25 mg/1 · Tablet, Film coated · Oral · Direct_Rx
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72189-364-30 | 72189036430 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-364-30)Marketed from Jun 21, 2022 |
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)
- Ropinirole
- Generic name (nonproprietary)
- ropinirole
- Active ingredients
- Ropinirole hydrochloride — .25 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Direct_Rx
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 204022
- Marketing start
- Listing expires
- Other FDA classes
- Dopamine Agonists (Mechanism)
- Identifiers
- Product ID 72189-364_2c4c8dd5-f07a-0339-e063-6394a90afedbSPL ID 2c4c8dd5-f07a-0339-e063-6394a90afedbSPL set ID e1fb0b51-4f8a-965d-e053-2a95a90ad936RxCUI 312845UNII 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
N472189036430followed by a unit qualifier and the quantityPackage 72189-0364-30. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 204022
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| ropinirole | Ropinirole hydrochloride 3 mg/1 | Tablet, Film coatedOral | Accord Healthcare Inc. | 16729-236 |
| ropinirole | Ropinirole hydrochloride 4 mg/1 | Tablet, Film coatedOral | Accord Healthcare Inc. | 16729-237 |
| ropinirole | Ropinirole hydrochloride 5 mg/1 | Tablet, Film coatedOral | Accord Healthcare Inc. | 16729-238 |
| ropinirole | Ropinirole hydrochloride .25 mg/1 | Tablet, Film coatedOral | Accord Healthcare Inc. | 16729-232 |
| ropinirole | Ropinirole hydrochloride 2 mg/1 | Tablet, Film coatedOral | Accord Healthcare Inc. | 16729-235 |
| ropinirole | Ropinirole hydrochloride .5 mg/1 | Tablet, Film coatedOral | Accord Healthcare Inc. | 16729-233 |
| ropinirole | Ropinirole hydrochloride 1 mg/1 | Tablet, Film coatedOral | Accord Healthcare Inc. | 16729-234 |
| ropinirole | Ropinirole hydrochloride .25 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-4803 |
| Ropinirole | Ropinirole hydrochloride 1 mg/1 | Tablet, Film coatedOral | DIRECT RX | 72189-222 |
| ropinirole | Ropinirole hydrochloride 2 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1167 |
| ropinirole | Ropinirole hydrochloride .5 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1188 |
| ropinirole | Ropinirole hydrochloride 1 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1982 |
| ropinirole | Ropinirole hydrochloride .25 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1231 |