What is NDC 70518-2987?

70518-2987 is the product NDC for Buspirone Hydrochloride, Buspirone hydrochloride 15 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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?

260 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 70518-2987

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-2987Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-2987Add 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
70518-2987-0	7051829870070518298700	30 TABLET in 1 BLISTER PACK (70518-2987-0)Marketed from Jan 12, 2021
70518-2987-2	7051829870270518298702	60 TABLET in 1 BLISTER PACK (70518-2987-2)Marketed from Jul 12, 2025

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): Buspirone Hydrochloride
Generic name (nonproprietary): buspirone hydrochloride
Active ingredients: Buspirone hydrochloride — 15 mg/1
Dosage form: Tablet
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075388
Marketing start: Jan 12, 2021
Listing expires: Dec 31, 2027
Identifiers: Product ID 70518-2987_57eb128e-2d03-c513-e063-6394a90a8d80SPL ID 57eb128e-2d03-c513-e063-6394a90a8d80SPL set ID 3155e607-bc7f-4e90-9edf-8e862dd5737dRxCUI 866018UNII 207LT9J9OC

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

N470518298700 followed by a unit qualifier and the quantity

Package 70518-2987-00. 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 Jul 31, 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 70518-2987

What is NDC 70518-2987?: 70518-2987 is the product NDC for Buspirone Hydrochloride, Buspirone hydrochloride 15 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 2 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?: REMEDYREPACK INC., NDC labeler code 70518. 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?: 260 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 5 mg/1	TabletOral	American Health Packaging	60687-988	60687-0988-01
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0285	55154-0285-00
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0286	55154-0286-00
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-018	87441-0018-01
Buspirone hydrochloride	Buspirone hydrochloride 15 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-019	87441-0019-01
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 12.5 mg/1	TabletOral	IPG Pharmaceuticals, Inc	71085-094	71085-0094-30
Buspirone Hydrochloride	Buspirone hydrochloride 2.5 mg/1	TabletOral	IPG Pharmaceuticals, Inc	71085-093	71085-0093-60
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Coupler LLC	67046-0645	67046-0645-03

All 261 Buspirone Hydrochloride NDCs

Other NDCs under ANDA 075388

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

FDA NDC Directory listings under ANDA 075388
Product	Strength	Form · route	Labeler	Product NDC
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	A-S Medication Solutions	50090-6649
Buspirone Hydrochloride	Buspirone hydrochloride 15 mg/1	TabletOral	A-S Medication Solutions	50090-7293
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	A-S Medication Solutions	50090-7682
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	A-S Medication Solutions	50090-7785
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Bryant Ranch Prepack	63629-2408
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Bryant Ranch Prepack	63629-2409
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-2410
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-2411
Buspirone Hydrochloride	Buspirone hydrochloride 15 mg/1	TabletOral	Bryant Ranch Prepack	63629-2412
Buspirone Hydrochloride	Buspirone hydrochloride 15 mg/1	TabletOral	Bryant Ranch Prepack	63629-2413
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-091
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-092
Buspirone Hydrochloride	Buspirone hydrochloride 15 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-093
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4443
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4586
Buspirone Hydrochloride	Buspirone hydrochloride 15 mg/1	TabletOral	Bryant Ranch Prepack	71335-1752
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-1938
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-9673
Buspirone Hydrochloride	Buspirone hydrochloride 5 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-943
Buspirone Hydrochloride	Buspirone hydrochloride 10 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-953

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