Prazosin Hydrochloride NDC 87441-068

NDC codes

FDA NDC Directory

Product NDC (as listed)87441-068Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87441-0068Add 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
87441-068-01	87441006801	30 CAPSULE in 1 BLISTER PACK (87441-068-01)Marketed from Jul 1, 2026

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): Prazosin Hydrochloride
Generic name (nonproprietary): prazosin hydrochloride
Active ingredients: Prazosin hydrochloride — 2 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Unit Dose Solutions, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213052
Marketing start: Jul 1, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)
Identifiers: Product ID 87441-068_5590970b-53cc-42e4-e063-6394a90a619bSPL ID 5590970b-53cc-42e4-e063-6394a90a619bSPL set ID 559082c2-4130-a2bc-e063-6294a90ab781RxCUI 312594UNII X0Z7454B90
Pharmacologic class: alpha-Adrenergic Blocker

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

N487441006801 followed by a unit qualifier and the quantity

Package 87441-0068-01. 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

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

Other NDCs under ANDA 213052

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

FDA NDC Directory listings under ANDA 213052
Product	Strength	Form · route	Labeler	Product NDC
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Aurobindo Pharma Limited	59651-271
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Aurobindo Pharma Limited	59651-272
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Aurobindo Pharma Limited	59651-273
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Aphena Pharma Solutions - Tennessee, LLC	71610-981
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Coupler LLC	67046-1678
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4489
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Unit Dose Solutions, Inc.	87441-067