NDC codes

FDA NDC Directory
Product NDC (as listed)76282-722Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76282-0722Add 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
76282-722-0176282072201100 CAPSULE in 1 BOTTLE (76282-722-01)Marketed from Jan 17, 2023
76282-722-10762820722101000 CAPSULE in 1 BOTTLE (76282-722-10)Marketed from Jan 17, 2023

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214608
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Antagonists (Mechanism)
Identifiers
Product ID 76282-722_f3388e9a-2c36-de8d-e053-2a95a90aa213SPL ID f3388e9a-2c36-de8d-e053-2a95a90aa213SPL set ID cdde7b22-6b29-4cac-8bd6-f613dab6eef1RxCUI 198141, 312593, 312594UNII X0Z7454B90UPC 0376282721019, 0376282722016, 0376282723013
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

N476282072201 followed by a unit qualifier and the quantity

Package 76282-0722-01. 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, USP 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 achi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 214608

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

FDA NDC Directory listings under ANDA 214608
ProductStrengthForm · routeLabelerProduct NDC
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralGranules Pharmaceuticals Inc.70010-084
Prazosin HydrochloridePrazosin hydrochloride 2 mg/1CapsuleOralGranules Pharmaceuticals Inc.70010-085
Prazosin HydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralGranules Pharmaceuticals Inc.70010-086
Prazosin HydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-829
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralExelan Pharmaceuticals76282-721
Prazosin HydrochloridePrazosin hydrochloride 1 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-693
Prazosin HydrochloridePrazosin hydrochloride 5 mg/1CapsuleOralExelan Pharmaceuticals76282-723
Prazosin HydrochloridePrazosin hydrochloride 2 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-694

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