What is NDC 82804-964?

82804-964 is the product NDC for Buspirone Hydrochloride, Buspirone hydrochloride 30 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 7 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 82804. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Buspirone Hydrochloride?

259 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Buspirone Hydrochloride NDC 82804-964 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)82804-964Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82804-0964Add 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
82804-964-00	82804096400	100 TABLET in 1 BOTTLE (82804-964-00)Marketed from Jan 12, 2026
82804-964-11	82804096411	1000 TABLET in 1 BOTTLE (82804-964-11)Marketed from Jan 12, 2026
82804-964-30	82804096430	30 TABLET in 1 BOTTLE (82804-964-30)Marketed from Jan 12, 2026
82804-964-55	82804096455	500 TABLET in 1 BOTTLE (82804-964-55)Marketed from Jan 12, 2026
82804-964-60	82804096460	60 TABLET in 1 BOTTLE (82804-964-60)Marketed from Jan 12, 2026
82804-964-72	82804096472	120 TABLET in 1 BOTTLE (82804-964-72)Marketed from Jan 12, 2026
82804-964-90	82804096490	90 TABLET in 1 BOTTLE (82804-964-90)Marketed from Jan 12, 2026

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): Buspirone Hydrochloride
Generic name (nonproprietary): buspirone hydrochloride
Active ingredients: Buspirone hydrochloride — 30 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 82804
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078302
Marketing start: May 1, 2020
Listing expires: Dec 31, 2027
Identifiers: Product ID 82804-964_1521109d-8386-472f-9483-f1fe9f7ed152SPL ID 1521109d-8386-472f-9483-f1fe9f7ed152SPL set ID 1521109d-8386-472f-9483-f1fe9f7ed152RxCUI 866018, 866083, 866090, 866094UNII 207LT9J9OCUPC 0382804962303, 0382804961306

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

N482804096400 followed by a unit qualifier and the quantity

Package 82804-0964-00. 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 Jan 1, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Buspirone hydrochloride tablets, USP are indicated for the management of anxiety disorders or the short-term relief of the symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. The efficacy of buspirone hydrochloride tablets, USP has been demonstrated in controlled clinical trials of outpatients whose diagnosis roughly corresponds to Generalized Anxiety Disorder (GAD). Many of the patients enrolled in these studies also had coexisting depressive symptoms and buspirone hydrochloride tablets, USP relieved anxiety in the presence of these coexisting depressive symptoms. The patients evalua…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82804-964

What is NDC 82804-964?: 82804-964 is the product NDC for Buspirone Hydrochloride, Buspirone hydrochloride 30 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Buspirone Hydrochloride.
What is the active ingredient?: Buspirone hydrochloride.
Who is the labeler?: Proficient Rx LP, NDC labeler code 82804. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Buspirone Hydrochloride?: 259 other product NDCs are listed under this name. See all Buspirone 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 Buspirone Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0286	55154-0286-00
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0285	55154-0285-00
Buspirone hydrochloride	Buspirone hydrochloride 15 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-019	87441-0019-01
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-018	87441-0018-01
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-020	87441-0020-01
Buspirone hydrochloride	Buspirone hydrochloride 7.5 mg/1	TabletOral	Coupler LLC	67046-1352	67046-1352-03
Buspirone Hydrochloride	Buspirone hydrochloride 2.5 mg/1	TabletOral	IPG Pharmaceuticals, Inc	71085-093	71085-0093-60
Buspirone Hydrochloride	Buspirone hydrochloride 12.5 mg/1	TabletOral	IPG Pharmaceuticals, Inc	71085-094	71085-0094-30
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Coupler LLC	67046-0645	67046-0645-03
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4586	70518-4586-00

All 260 Buspirone Hydrochloride NDCs

Other NDCs under ANDA 078302

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

FDA NDC Directory listings under ANDA 078302
Product	Strength	Form · route	Labeler	Product NDC
Buspirone Hydrochloride	Buspirone hydrochloride 30 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-142
Buspirone Hydrochloride	Buspirone hydrochloride 30 mg/1	TabletOral	Bryant Ranch Prepack	71335-2768
Buspirone Hydrochloride	Buspirone hydrochloride 30 mg/1	TabletOral	Bryant Ranch Prepack	63629-2414
Buspirone Hydrochloride	Buspirone hydrochloride 30 mg/1	TabletOral	Bryant Ranch Prepack	63629-2415
Buspirone Hydrochloride	Buspirone hydrochloride 30 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-094
Buspirone Hydrochloride	Buspirone hydrochloride 30 mg/1	TabletOral	Bryant Ranch Prepack	72162-1927
Buspirone Hydrochloride	Buspirone hydrochloride 30 mg/1	TabletOral	A-S Medication Solutions	50090-7742