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 NDC11-digit (billing)PackageCopy
87441-068-01874410068018744100680130 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.NDC labeler code 87441
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213052
Marketing start
Listing expires
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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Prazosin hydrochloride capsules are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes, including this drug. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than one drug to achieve b…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87441-068

What is NDC 87441-068?
87441-068 is the product NDC for Prazosin Hydrochloride, Prazosin hydrochloride 2 mg/1 capsule, listed with the FDA by Unit Dose Solutions, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Prazosin Hydrochloride.
What is the active ingredient?
Prazosin hydrochloride.
Who is the labeler?
Unit Dose Solutions, Inc., NDC labeler code 87441. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Prazosin Hydrochloride?
104 other product NDCs are listed under this name. See all Prazosin Hydrochloride 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 Prazosin Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
prazosin hydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralCoupler LLC67046-105067046-1050-03
prazosin hydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralREMEDYREPACK INC.70518-471270518-4712-00
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-06787441-0067-01
Prazosin HydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralCoupler LLC67046-078167046-0781-03
Prazosin HydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralCoupler LLC67046-167867046-1678-03
Prazosin HydrochloridePrazosin hydrochloride 2 mg/1CapsuleOralCoupler LLC67046-050467046-0504-03
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralCoupler LLC67046-068067046-0680-03
Prazosin HydrochloridePrazosin hydrochloride 2 mg/1CapsuleOralSafecor Health LLC48433-08548433-0085-20
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralSafecor Health LLC48433-08448433-0084-20
Prazosin HydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralSafecor Health LLC48433-08648433-0086-20

All 105 Prazosin Hydrochloride NDCs

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
ProductStrengthForm · routeLabelerProduct NDC
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralAurobindo Pharma Limited59651-271
Prazosin HydrochloridePrazosin hydrochloride 2 mg/1CapsuleOralAurobindo Pharma Limited59651-272
Prazosin HydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralAurobindo Pharma Limited59651-273
Prazosin HydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralCoupler LLC67046-1678
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralREMEDYREPACK INC.70518-4489
Prazosin HydrochloridePrazosin hydrochloride 2 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-981
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-067

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