NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0584Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0584Add 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
71335-0584-17133505840190 TABLET in 1 BOTTLE (71335-0584-1)Marketed from Jul 2, 2018
71335-0584-27133505840230 TABLET in 1 BOTTLE (71335-0584-2)Marketed from Apr 24, 2018
71335-0584-37133505840360 TABLET in 1 BOTTLE (71335-0584-3)Marketed from May 2, 2022

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)
Pramipexole Dihydrochloride
Generic name (nonproprietary)
pramipexole dihydrochloride
Active ingredients
Pramipexole dihydrochloride — .5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090865
Marketing start
Listing expires
Other FDA classes
Dopamine Agonists (Mechanism)
Identifiers
Product ID 71335-0584_b042def2-13f3-48c8-9a05-5b56ab536372SPL ID b042def2-13f3-48c8-9a05-5b56ab536372SPL set ID 350a3f84-0f98-405f-bdae-6abbc47d48a4RxCUI 859044UNII 3D867NP06J
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

N471335058401 followed by a unit qualifier and the quantity

Package 71335-0584-01. 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 .

Indications (excerpt from the label)

Pramipexole dihydrochloride is a non-ergot dopamine agonist indicated for the treatment of: Parkinson's disease (PD) (1.1) Moderate-to-severe primary Restless Legs Syndrome (RLS) (1.2) 1.1 Parkinson’s Disease Pramipexole dihydrochloride tablets are indicated for the treatment of Parkinson's disease. 1.2 Restless Legs Syndrome Pramipexole dihydrochloride 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)

Other NDCs under ANDA 090865

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

FDA NDC Directory listings under ANDA 090865
ProductStrengthForm · routeLabelerProduct NDC
Pramipexole DihydrochloridePramipexole dihydrochloride .75 mg/1TabletOralTorrent Pharmaceuticals Limited13668-184
Pramipexole DihydrochloridePramipexole dihydrochloride .25 mg/1TabletOralAmerican Health Packaging60687-570
Pramipexole DihydrochloridePramipexole dihydrochloride .5 mg/1TabletOralAmerican Health Packaging60687-581
Pramipexole DihydrochloridePramipexole dihydrochloride 1 mg/1TabletOralAmerican Health Packaging60687-592
Pramipexole DihydrochloridePramipexole dihydrochloride 1 mg/1TabletOralBryant Ranch Prepack71335-2167
Pramipexole DihydrochloridePramipexole dihydrochloride .25 mg/1TabletOralBryant Ranch Prepack63629-5013
Pramipexole DihydrochloridePramipexole dihydrochloride .125 mg/1TabletOralBryant Ranch Prepack63629-5042
Pramipexole DihydrochloridePramipexole dihydrochloride .75 mg/1TabletOralBryant Ranch Prepack72162-2569
Pramipexole DihydrochloridePramipexole dihydrochloride 1.5 mg/1TabletOralA-S Medication Solutions50090-7816
Pramipexole DihydrochloridePramipexole dihydrochloride .25 mg/1TabletOralMajor Pharmaceuticals0904-6704
Pramipexole DihydrochloridePramipexole dihydrochloride .25 mg/1TabletOralTorrent Pharmaceuticals Limited13668-092
Pramipexole DihydrochloridePramipexole dihydrochloride .125 mg/1TabletOralTorrent Pharmaceuticals Limited13668-091
Pramipexole DihydrochloridePramipexole dihydrochloride .5 mg/1TabletOralTorrent Pharmaceuticals Limited13668-093
Pramipexole DihydrochloridePramipexole dihydrochloride 1 mg/1TabletOralTorrent Pharmaceuticals Limited13668-094
Pramipexole DihydrochloridePramipexole dihydrochloride 1.5 mg/1TabletOralTorrent Pharmaceuticals Limited13668-095

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