What is NDC 71335-2793?

71335-2793 is the product NDC for Ropinirole, Ropinirole hydrochloride .25 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ropinirole?

110 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ropinirole NDC 71335-2793 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2793Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2793Add 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
71335-2793-1	7133527930171335279301	30 TABLET, FILM COATED in 1 BOTTLE (71335-2793-1)Marketed from Mar 11, 2026
71335-2793-2	7133527930271335279302	60 TABLET, FILM COATED in 1 BOTTLE (71335-2793-2)Marketed from Mar 11, 2026
71335-2793-3	7133527930371335279303	28 TABLET, FILM COATED in 1 BOTTLE (71335-2793-3)Marketed from Mar 11, 2026
71335-2793-4	7133527930471335279304	100 TABLET, FILM COATED in 1 BOTTLE (71335-2793-4)Marketed from Mar 11, 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): Ropinirole
Generic name (nonproprietary): ropinirole
Active ingredients: Ropinirole hydrochloride — .25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 079229
Marketing start: Sep 15, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Dopamine Agonists (Mechanism)
Identifiers: Product ID 71335-2793_3bb5d006-f98d-43e3-8884-14cb5c367db9SPL ID 3bb5d006-f98d-43e3-8884-14cb5c367db9SPL set ID 245fc49d-609e-4431-b8fa-668b39d12ec2RxCUI 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

N471335279301 followed by a unit qualifier and the quantity

Package 71335-2793-01. 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 Mar 11, 2026.

Indications (excerpt from the label)

Ropinirole tablets are a non-ergoline dopamine agonist indicated for the treatment of Parkinson’s disease (PD) and moderate-to-severe primary Restless Legs Syndrome (RLS). (1.1, 1.2) 1.1 Parkinson’s Disease Ropinirole tablets are indicated for the treatment of Parkinson’s disease. 1.2 Restless Legs Syndrome Ropinirole tablets are indicated for the treatment of moderate-to-severe primary Restless Legs Syndrome (RLS).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2793

What is NDC 71335-2793?: 71335-2793 is the product NDC for Ropinirole, Ropinirole hydrochloride .25 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ropinirole.
What is the active ingredient?: Ropinirole hydrochloride.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ropinirole?: 110 other product NDCs are listed under this name. See all Ropinirole 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 Ropinirole NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
ropinirole	Ropinirole hydrochloride 2 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4138	68788-4138-03
Ropinirole	Ropinirole hydrochloride 2 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2602	72162-2602-0372162-2602-09
Ropinirole	Ropinirole hydrochloride 4 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2603	72162-2603-0372162-2603-09
Ropinirole	Ropinirole hydrochloride 6 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2604	72162-2604-0372162-2604-09
Ropinirole	Ropinirole hydrochloride 8 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2605	72162-2605-0372162-2605-09
Ropinirole	Ropinirole hydrochloride 12 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	72162-2606	72162-2606-0372162-2606-09
Ropinirole	Ropinirole hydrochloride 2 mg/1	Tablet, Extended releaseOral	Elite Laboratories, Inc.	64850-250	64850-0250-30
Ropinirole	Ropinirole hydrochloride 4 mg/1	Tablet, Extended releaseOral	Elite Laboratories, Inc.	64850-251	64850-0251-30
Ropinirole	Ropinirole hydrochloride 6 mg/1	Tablet, Extended releaseOral	Elite Laboratories, Inc.	64850-252	64850-0252-30
Ropinirole	Ropinirole hydrochloride 8 mg/1	Tablet, Extended releaseOral	Elite Laboratories, Inc.	64850-253	64850-0253-30

All 111 Ropinirole NDCs

Other NDCs under ANDA 079229

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

FDA NDC Directory listings under ANDA 079229
Product	Strength	Form · route	Labeler	Product NDC
Ropinirole	Ropinirole hydrochloride 4 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7445
Ropinirole	Ropinirole hydrochloride .25 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-356
Ropinirole	Ropinirole hydrochloride .5 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-357
Ropinirole	Ropinirole hydrochloride 1 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-358
Ropinirole	Ropinirole hydrochloride 2 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-359
Ropinirole	Ropinirole hydrochloride 3 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-360
Ropinirole	Ropinirole hydrochloride 4 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-361
Ropinirole	Ropinirole hydrochloride 5 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-362
Ropinirole	Ropinirole hydrochloride .5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4318
Ropinirole	Ropinirole hydrochloride 2 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2515
Ropinirole	Ropinirole hydrochloride .5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-9653
Ropinirole	Ropinirole hydrochloride 1 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-9656
Ropinirole	Ropinirole hydrochloride .5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-2200
Ropinirole	Ropinirole hydrochloride 1 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-494
Ropinirole	Ropinirole hydrochloride .25 mg/1	Tablet, Film coatedOral	ASCLEMED USA INC.	87063-198
Ropinirole	Ropinirole hydrochloride .5 mg/1	Tablet, Film coatedOral	ASCLEMED USA INC.	87063-199
Ropinirole	Ropinirole hydrochloride 1 mg/1	Tablet, Film coatedOral	ASCLEMED USA INC.	87063-200
Ropinirole	Ropinirole hydrochloride 2 mg/1	Tablet, Film coatedOral	ASCLEMED USA INC.	87063-201