What is NDC 71335-9648?

71335-9648 is the product NDC for prazosin hydrochloride, Prazosin hydrochloride 1 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 5 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

prazosin hydrochloride NDC 71335-9648

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-9648Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-9648Add 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
71335-9648-1	7133596480171335964801	30 CAPSULE in 1 BOTTLE (71335-9648-1)Marketed from Feb 21, 2023
71335-9648-2	7133596480271335964802	100 CAPSULE in 1 BOTTLE (71335-9648-2)Marketed from Feb 21, 2023
71335-9648-3	7133596480371335964803	60 CAPSULE in 1 BOTTLE (71335-9648-3)Marketed from Feb 21, 2023
71335-9648-4	7133596480471335964804	28 CAPSULE in 1 BOTTLE (71335-9648-4)Marketed from Feb 21, 2023
71335-9648-5	7133596480571335964805	90 CAPSULE in 1 BOTTLE (71335-9648-5)Marketed from Feb 21, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 1 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215697
Marketing start: Jan 3, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)
Identifiers: Product ID 71335-9648_c6d0eacc-75e7-4446-8029-61a2024f496cSPL ID c6d0eacc-75e7-4446-8029-61a2024f496cSPL set ID fa00e99e-f050-4544-a11b-d20c9710761eRxCUI 312593UNII 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

N471335964801 followed by a unit qualifier and the quantity

Package 71335-9648-01. 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 Jul 3, 2025.

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 71335-9648

What is NDC 71335-9648?: 71335-9648 is the product NDC for prazosin hydrochloride, Prazosin hydrochloride 1 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 5 package NDCs, 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
prazosin hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Coupler LLC	67046-1050	67046-1050-03
prazosin hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4712	70518-4712-00
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Unit Dose Solutions, Inc.	87441-067	87441-0067-01
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Unit Dose Solutions, Inc.	87441-068	87441-0068-01
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Coupler LLC	67046-0781	67046-0781-03
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Coupler LLC	67046-1678	67046-1678-03
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Coupler LLC	67046-0504	67046-0504-03
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Coupler LLC	67046-0680	67046-0680-03
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Safecor Health LLC	48433-085	48433-0085-20
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Safecor Health LLC	48433-084	48433-0084-20

All 105 prazosin hydrochloride NDCs

Other NDCs under ANDA 215697

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

FDA NDC Directory listings under ANDA 215697
Product	Strength	Form · route	Labeler	Product NDC
Prazosin HCL	Prazosin hydrochloride 1 mg/1	CapsuleOral	Direct_Rx	72189-436
Prazosin HCL	Prazosin hydrochloride 5 mg/1	CapsuleOral	Direct_Rx	72189-470
Prazosin HCL	Prazosin hydrochloride 2 mg/1	CapsuleOral	Direct_Rx	72189-540
prazosin hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	ST. MARY'S MEDICAL PARK PHARMACY	60760-820
prazosin hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	ST. MARY'S MEDICAL PARK PHARMACY	60760-821
prazosin hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Coupler LLC	67046-1050
prazosin hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Coupler, LLC	67046-1532
prazosin hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	NuCare Pharmaceuticals,Inc.	68071-2972
prazosin hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-8660
prazosin hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3669
prazosin hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3679
prazosin hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4288
prazosin hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Lifestar Pharma LLC	70756-429
prazosin hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Lifestar Pharma LLC	70756-430
prazosin hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Lifestar Pharma LLC	70756-440
prazosin hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2311
prazosin hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2348
prazosin hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	ASCLEMED USA INC.	76420-523
prazosin hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	ASCLEMED USA INC.	76420-525
prazosin hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	ASCLEMED USA INC.	76420-526

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