What is NDC 70010-084?

70010-084 is the product NDC for Prazosin Hydrochloride, Prazosin hydrochloride 1 mg/1 capsule, listed with the FDA by Granules Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Granules Pharmaceuticals Inc., NDC labeler code 70010. 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 70010-084

NDC codes

FDA NDC Directory

Product NDC (as listed)70010-084Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70010-0084Add 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	Copy
70010-084-01	7001000840170010008401	100 CAPSULE in 1 BOTTLE (70010-084-01)Marketed from Jan 3, 2022
70010-084-10	7001000841070010008410	1000 CAPSULE in 1 BOTTLE (70010-084-10)Marketed from Jan 3, 2022

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 — 1 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Granules Pharmaceuticals Inc.NDC labeler code 70010
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214608
Marketing start: Jan 3, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Antagonists (Mechanism)
Identifiers: Product ID 70010-084_5d4ebfee-36e5-3385-e063-6294a90a5ef2SPL ID 5d4ebfee-36e5-3385-e063-6294a90a5ef2
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

N470010008401 followed by a unit qualifier and the quantity

Package 70010-0084-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70010-084

What is NDC 70010-084?: 70010-084 is the product NDC for Prazosin Hydrochloride, Prazosin hydrochloride 1 mg/1 capsule, listed with the FDA by Granules Pharmaceuticals Inc.. It has 2 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?: Granules Pharmaceuticals Inc., NDC labeler code 70010. 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 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
Product	Strength	Form · route	Labeler	Product NDC
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Granules Pharmaceuticals Inc.	70010-085
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Granules Pharmaceuticals Inc.	70010-086
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Aphena Pharma Solutions - Tennessee, LLC	71610-693
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Aphena Pharma Solutions - Tennessee, LLC	71610-694
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Aphena Pharma Solutions - Tennessee, LLC	71610-829
Prazosin Hydrochloride	Prazosin hydrochloride 1 mg/1	CapsuleOral	Exelan Pharmaceuticals	76282-721
Prazosin Hydrochloride	Prazosin hydrochloride 2 mg/1	CapsuleOral	Exelan Pharmaceuticals	76282-722
Prazosin Hydrochloride	Prazosin hydrochloride 5 mg/1	CapsuleOral	Exelan Pharmaceuticals	76282-723