pramipexole dihydrochloride NDC 29300-211

NDC codes

FDA NDC Directory

Product NDC (as listed)29300-211Labeler and product segments. Claims need a package NDC.

Product NDC at billing width29300-0211Add 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
29300-211-10	29300021110	1000 TABLET in 1 BOTTLE, PLASTIC (29300-211-10)Marketed from Mar 1, 2019
29300-211-19	29300021119	90 TABLET in 1 BOTTLE, PLASTIC (29300-211-19)Marketed from Mar 1, 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 — 1.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Unichem Pharmaceuticals (USA), Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207011
Marketing start: Mar 1, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Dopamine Agonists (Mechanism)
Identifiers: Product ID 29300-211_2ab8bb44-e4ba-4ae0-8ce9-0e9153de59f3SPL ID 2ab8bb44-e4ba-4ae0-8ce9-0e9153de59f3SPL set ID b978aa75-c62d-444b-9ec6-6c0d21a66688RxCUI 858625, 859033, 859040, 859044, 859048, 859052UNII 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

N429300021110 followed by a unit qualifier and the quantity

Package 29300-0211-10. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 207011

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

FDA NDC Directory listings under ANDA 207011
Product	Strength	Form · route	Labeler	Product NDC
pramipexole dihydrochloride	Pramipexole dihydrochloride .125 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-207
pramipexole dihydrochloride	Pramipexole dihydrochloride .25 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-208
pramipexole dihydrochloride	Pramipexole dihydrochloride .5 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-209
pramipexole dihydrochloride	Pramipexole dihydrochloride 1 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-210
pramipexole dihydrochloride	Pramipexole dihydrochloride .75 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-270