What is NDC 62332-159?

62332-159 is the product NDC for Pramipexole Dihydrochloride, Pramipexole dihydrochloride 4.5 mg/1 tablet, extended release, listed with the FDA by Alembic Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Alembic Pharmaceuticals Inc., NDC labeler code 62332. 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 Dihydrochloride?

127 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pramipexole Dihydrochloride NDC 62332-159

NDC codes

FDA NDC Directory

Product NDC (as listed)62332-159Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62332-0159Add 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	Copy
62332-159-30	6233201593062332015930	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-159-30)Marketed from Jan 3, 2019

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 Dihydrochloride
Generic name (nonproprietary): pramipexole dihydrochloride
Active ingredients: Pramipexole dihydrochloride — 4.5 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Alembic Pharmaceuticals Inc.NDC labeler code 62332
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204518
Marketing start: Jan 3, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Dopamine Agonists (Mechanism)
Identifiers: Product ID 62332-159_3e5d0f03-6a98-44eb-8bb5-366364812d50SPL ID 3e5d0f03-6a98-44eb-8bb5-366364812d50SPL set ID e18b67b6-a085-43e5-bb2b-fe74fa00cb65RxCUI 901534, 901541, 901546, 901550, 901555, 1114479, 1114485UNII 3D867NP06JUPC 0362332154302, 0362332155309, 0362332158300, 0362332156306, 0362332160303, 0362332157303, 0362332159307
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

N462332015930 followed by a unit qualifier and the quantity

Package 62332-0159-30. 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

Current FDA label (SPL), effective Jun 20, 2024.

Indications (excerpt from the label)

Pramipexole dihydrochloride extended-release tablets are indicated for the treatment of Parkinson’s disease. Pramipexole dihydrochloride is a non-ergot dopamine agonist indicated for the treatment of Parkinson’s disease (PD)(1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62332-159

What is NDC 62332-159?: 62332-159 is the product NDC for Pramipexole Dihydrochloride, Pramipexole dihydrochloride 4.5 mg/1 tablet, extended release, listed with the FDA by Alembic Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pramipexole Dihydrochloride.
What is the active ingredient?: Pramipexole dihydrochloride.
Who is the labeler?: Alembic Pharmaceuticals Inc., NDC labeler code 62332. 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 Dihydrochloride?: 127 other product NDCs are listed under this name. See all Pramipexole Dihydrochloride 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 Dihydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pramipexole dihydrochloride	Pramipexole dihydrochloride .375 mg/1	Tablet, Extended releaseOral	Ingenus Pharmaceuticals, LLC	50742-331	50742-0331-30
Pramipexole dihydrochloride	Pramipexole dihydrochloride 2.25 mg/1	Tablet, Extended releaseOral	Ingenus Pharmaceuticals, LLC	50742-334	50742-0334-30
Pramipexole dihydrochloride	Pramipexole dihydrochloride .75 mg/1	Tablet, Extended releaseOral	Ingenus Pharmaceuticals, LLC	50742-332	50742-0332-30
Pramipexole dihydrochloride	Pramipexole dihydrochloride 1.5 mg/1	Tablet, Extended releaseOral	Ingenus Pharmaceuticals, LLC	50742-333	50742-0333-30
Pramipexole dihydrochloride	Pramipexole dihydrochloride 3 mg/1	Tablet, Extended releaseOral	Ingenus Pharmaceuticals, LLC	50742-335	50742-0335-30
Pramipexole dihydrochloride	Pramipexole dihydrochloride 3.75 mg/1	Tablet, Extended releaseOral	Ingenus Pharmaceuticals, LLC	50742-336	50742-0336-30
Pramipexole dihydrochloride	Pramipexole dihydrochloride 4.5 mg/1	Tablet, Extended releaseOral	Ingenus Pharmaceuticals, LLC	50742-337	50742-0337-30
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .75 mg/1	Tablet, Extended releaseOral	Vitruvias Therapeutics, Inc.	69680-146	69680-0146-30
pramipexole dihydrochloride	Pramipexole dihydrochloride .125 mg/1	TabletOral	Strides Pharma Science Limited	64380-746	64380-0746-05
pramipexole dihydrochloride	Pramipexole dihydrochloride 1 mg/1	TabletOral	Strides Pharma Science Limited	64380-750	64380-0750-0164380-0750-05

All 128 Pramipexole Dihydrochloride NDCs

Other NDCs under ANDA 204518

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

FDA NDC Directory listings under ANDA 204518
Product	Strength	Form · route	Labeler	Product NDC
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .375 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-574
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .75 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-575
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 1.5 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-576
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 2.25 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-577
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 3 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-578
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 3.75 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-579
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 4.5 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-580
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .375 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Inc.	62332-154
Pramipexole Dihydrochloride	Pramipexole dihydrochloride .75 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Inc.	62332-155
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 1.5 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Inc.	62332-156
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 2.25 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Inc.	62332-157
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 3 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Inc.	62332-158
Pramipexole Dihydrochloride	Pramipexole dihydrochloride 3.75 mg/1	Tablet, Extended releaseOral	Alembic Pharmaceuticals Inc.	62332-160