What is NDC 0093-4069?

0093-4069 is the product NDC for Prazosin Hydrochloride, Prazosin hydrochloride 5 mg/1 capsule, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. 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 0093-4069 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0093-4069Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00093-4069Add 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
0093-4069-01	00093406901	100 CAPSULE in 1 BOTTLE (0093-4069-01)Marketed from Feb 22, 2007
0093-4069-05	00093406905	500 CAPSULE in 1 BOTTLE (0093-4069-05)Marketed from Jan 18, 2007
0093-4069-52	00093406952	250 CAPSULE in 1 BOTTLE (0093-4069-52)Marketed from Feb 22, 2007

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 5 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Teva Pharmaceuticals USA, Inc.NDC labeler code 0093
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 071745
Marketing start: Jan 18, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)
Identifiers: Product ID 0093-4069_b9dbf961-8602-4533-90ad-8e5cf16e6649SPL ID b9dbf961-8602-4533-90ad-8e5cf16e6649SPL set ID 7293cef3-ef9e-40dc-9995-875ef047f693RxCUI 198141, 312593, 312594UNII X0Z7454B90UPC 0300934068016, 0300934069013, 0300934067019
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

N400093406901 followed by a unit qualifier and the quantity

Package 00093-4069-01. 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 Oct 25, 2018.

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 0093-4069

What is NDC 0093-4069?: 0093-4069 is the product NDC for Prazosin Hydrochloride, Prazosin hydrochloride 5 mg/1 capsule, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 3 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?: Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. 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 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 1 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-7335
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