What is NDC 31722-909?

31722-909 is the product NDC for Pramipexole, Pramipexole dihydrochloride .75 mg/1 tablet, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pramipexole?

5 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pramipexole NDC 31722-909 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)31722-909Labeler and product segments. Claims need a package NDC.

Product NDC at billing width31722-0909Add 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
31722-909-05	3172209090531722090905	500 TABLET in 1 BOTTLE (31722-909-05)Marketed from Aug 1, 2015
31722-909-10	3172209091031722090910	1000 TABLET in 1 BOTTLE (31722-909-10)Marketed from Aug 1, 2015
31722-909-90	3172209099031722090990	90 TABLET in 1 BOTTLE (31722-909-90)Marketed from Aug 1, 2015

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): Pramipexole
Generic name (nonproprietary): pramipexole
Active ingredients: Pramipexole dihydrochloride — .75 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Camber Pharmaceuticals, Inc.NDC labeler code 31722
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203855
Marketing start: Aug 1, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Dopamine Agonists (Mechanism)
Identifiers: Product ID 31722-909_540a17f8-b64d-41e1-a96b-d55bc8c48f3dSPL ID 540a17f8-b64d-41e1-a96b-d55bc8c48f3dSPL set ID a7405a56-de1c-4875-b57f-210c991474baRxCUI 858625, 859033, 859040, 859044, 859048, 859052UNII 3D867NP06JUPC 0331722906906
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

N431722090905 followed by a unit qualifier and the quantity

Package 31722-0909-05. 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 Oct 13, 2016.

Indications (excerpt from the label)

PRAMIPEXOLE DIHYDROCHLORIDE tablets is a non-ergot dopamine agonist indicated for the treatment of • the signs and symptoms of idiopathic Parkinson's disease (PD) ( 1.1 ) 1.1 Parkinson's Disease Pramipexole dihydrochloride tablets are indicated for the treatment of the signs and symptoms of idiopathic Parkinson's disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 31722-909

What is NDC 31722-909?: 31722-909 is the product NDC for Pramipexole, Pramipexole dihydrochloride .75 mg/1 tablet, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pramipexole.
What is the active ingredient?: Pramipexole dihydrochloride.
Who is the labeler?: Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pramipexole?: 5 other product NDCs are listed under this name. See all Pramipexole 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 Pramipexole NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pramipexole	Pramipexole dihydrochloride .125 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-906	31722-0906-0531722-0906-1031722-0906-90
Pramipexole	Pramipexole dihydrochloride .25 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-907	31722-0907-0531722-0907-1031722-0907-90
Pramipexole	Pramipexole dihydrochloride .5 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-908	31722-0908-0531722-0908-1031722-0908-90
Pramipexole	Pramipexole dihydrochloride 1 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-910	31722-0910-0531722-0910-1031722-0910-90
Pramipexole	Pramipexole dihydrochloride 1.5 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-911	31722-0911-0531722-0911-1031722-0911-90

Other NDCs under ANDA 203855

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

FDA NDC Directory listings under ANDA 203855
Product	Strength	Form · route	Labeler	Product NDC
Pramipexole	Pramipexole dihydrochloride .125 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-906
Pramipexole	Pramipexole dihydrochloride .25 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-907
Pramipexole	Pramipexole dihydrochloride .5 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-908
Pramipexole	Pramipexole dihydrochloride 1 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-910
Pramipexole	Pramipexole dihydrochloride 1.5 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-911
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .125 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-126
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .25 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-127
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .5 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-128
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .75 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-129
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 1 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-130
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 1.5 mg/1	TabletOral	ScieGen Pharmaceuticals Inc	50228-131
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .125 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-085
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .25 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-086
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .5 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-087
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .75 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-088
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 1 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-089
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 1.5 mg/1	TabletOral	Golden State Medical Supply, Inc.	60429-090