What is NDC 68788-7335?

68788-7335 is the product NDC for Prazosin Hydrochloride, Prazosin hydrochloride 1 mg/1 capsule, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 68788-7335

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-7335Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-7335Add 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
68788-7335-1	6878873350168788733501	100 CAPSULE in 1 BOTTLE (68788-7335-1)Marketed from Mar 12, 2019
68788-7335-3	6878873350368788733503	30 CAPSULE in 1 BOTTLE (68788-7335-3)Marketed from Mar 12, 2019
68788-7335-6	6878873350668788733506	60 CAPSULE in 1 BOTTLE (68788-7335-6)Marketed from Mar 12, 2019
68788-7335-9	6878873350968788733509	90 CAPSULE in 1 BOTTLE (68788-7335-9)Marketed from Mar 12, 2019

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: Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 071745
Marketing start: Mar 12, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)
Identifiers: Product ID 68788-7335_45408ca7-c073-451a-92d4-5d574f8c49e7SPL ID 45408ca7-c073-451a-92d4-5d574f8c49e7SPL set ID c8202658-422f-41db-bdee-7bb95b972b32RxCUI 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

N468788733501 followed by a unit qualifier and the quantity

Package 68788-7335-01. 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 Aug 17, 2026.

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 achie…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-7335

What is NDC 68788-7335?: 68788-7335 is the product NDC for Prazosin Hydrochloride, Prazosin hydrochloride 1 mg/1 capsule, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 4 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?: Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 1 mg/1	CapsuleOral	Safecor Health LLC	48433-084	48433-0084-20
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Safecor Health LLC	48433-085	48433-0085-20

All 105 Prazosin Hydrochloride NDCs

Other NDCs under ANDA 071745

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

FDA NDC Directory listings under ANDA 071745
Product	Strength	Form · route	Labeler	Product NDC
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Teva Pharmaceuticals USA, Inc.	0093-4067
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Teva Pharmaceuticals USA, Inc.	0093-4068
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Teva Pharmaceuticals USA, Inc.	0093-4069
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-8181
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	American Health Packaging	60687-572
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-8750
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-8756
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	American Health Packaging	68084-996
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	American Health Packaging	68084-997
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3352
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Proficient Rx LP	71205-585