NDC codes

FDA NDC Directory
Product NDC (as listed)71085-093Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71085-0093Add 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 NDC11-digit (billing)PackageCopy
71085-093-607108500936060 TABLET in 1 BOTTLE (71085-093-60)Marketed from May 29, 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 — 2.5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208972
Marketing start
Listing expires
Identifiers
Product ID 71085-093_54ce3b90-d11a-cd1e-e063-6294a90a2753SPL ID 54ce3b90-d11a-cd1e-e063-6294a90a2753SPL set ID 2c516eec-65d9-4481-8823-ae6b6da84062RxCUI 2744290, 2744292UNII 207LT9J9OCUPC 0371085093608, 0371085094308

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

N471085009360 followed by a unit qualifier and the quantity

Package 71085-0093-60. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Buspirone hydrochloride tablets 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 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 relieved anxiety in the presence of these coexisting depressive symptoms. The patients evaluated in these st…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208972

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

FDA NDC Directory listings under ANDA 208972
ProductStrengthForm · routeLabelerProduct NDC
Buspirone HydrochlorideBuspirone hydrochloride 7.5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-404
Buspirone HydrochlorideBuspirone hydrochloride 5 mg/1TabletOralEpic Pharma, LLC42806-082
Buspirone HydrochlorideBuspirone hydrochloride 15 mg/1TabletOralEpic Pharma, LLC42806-085
Buspirone HydrochlorideBuspirone hydrochloride 7.5 mg/1TabletOralEpic Pharma, LLC42806-083
Buspirone HydrochlorideBuspirone hydrochloride 10 mg/1TabletOralEpic Pharma, LLC42806-084
Buspirone HydrochlorideBuspirone hydrochloride 30 mg/1TabletOralEpic Pharma, LLC42806-086
Buspirone HydrochlorideBuspirone hydrochloride 12.5 mg/1TabletOralIPG Pharmaceuticals, Inc71085-094

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