NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2602Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2602Add 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 NDC11-digit (billing)PackageCopy
72162-2602-3721622602037216226020330 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2602-3)Marketed from Apr 17, 2026
72162-2602-9721622602097216226020990 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2602-9)Marketed from Apr 17, 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 — 2 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217862
Marketing start
Listing expires
Other FDA classes
Dopamine Agonists (Mechanism)
Identifiers
Product ID 72162-2602_103ad62b-798a-4697-883e-dc71ebcc9897SPL ID 103ad62b-798a-4697-883e-dc71ebcc9897SPL set ID 518e7407-8ef2-4596-8218-c318b4fd7634RxCUI 799055UNII 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

N472162260203 followed by a unit qualifier and the quantity

Package 72162-2602-03. 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 .

Indications (excerpt from the label)

Ropinirole extended-release tablets are indicated for the treatment of Parkinson's disease. Ropinirole extended-release tablets are non-ergoline dopamine agonist indicated for the treatment of Parkinson’s disease. ( 1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2602

What is NDC 72162-2602?
72162-2602 is the product NDC for Ropinirole, Ropinirole hydrochloride 2 mg/1 tablet, extended release, listed with the FDA by Bryant Ranch Prepack. It has 2 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 72162. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ropiniroleRopinirole hydrochloride 2 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-413868788-4138-03
RopiniroleRopinirole hydrochloride 4 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-260372162-2603-0372162-2603-09
RopiniroleRopinirole hydrochloride 6 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-260472162-2604-0372162-2604-09
RopiniroleRopinirole hydrochloride 8 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-260572162-2605-0372162-2605-09
RopiniroleRopinirole hydrochloride 12 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-260672162-2606-0372162-2606-09
RopiniroleRopinirole hydrochloride 2 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-25064850-0250-30
RopiniroleRopinirole hydrochloride 4 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-25164850-0251-30
RopiniroleRopinirole hydrochloride 6 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-25264850-0252-30
RopiniroleRopinirole hydrochloride 8 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-25364850-0253-30
RopiniroleRopinirole hydrochloride 12 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-25464850-0254-30

All 111 Ropinirole NDCs

Other NDCs under ANDA 217862

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

FDA NDC Directory listings under ANDA 217862
ProductStrengthForm · routeLabelerProduct NDC
RopiniroleRopinirole hydrochloride 2 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-250
RopiniroleRopinirole hydrochloride 4 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-251
RopiniroleRopinirole hydrochloride 6 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-252
RopiniroleRopinirole hydrochloride 8 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-253
RopiniroleRopinirole hydrochloride 12 mg/1Tablet, Extended releaseOralElite Laboratories, Inc.64850-254
RopiniroleRopinirole hydrochloride 4 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-2603
RopiniroleRopinirole hydrochloride 6 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-2604
RopiniroleRopinirole hydrochloride 8 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-2605
RopiniroleRopinirole hydrochloride 12 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-2606

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