NDC codes

FDA NDC Directory
Product NDC (as listed)71205-280Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0280Add 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
71205-280-307120502803030 TABLET in 1 BOTTLE (71205-280-30)Marketed from Jun 1, 2019
71205-280-607120502806060 TABLET in 1 BOTTLE (71205-280-60)Marketed from Jun 1, 2019
71205-280-907120502809090 TABLET in 1 BOTTLE (71205-280-90)Marketed from Jun 1, 2019

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 — 15 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209696
Marketing start
Listing expires
Identifiers
Product ID 71205-280_b02f563b-a2cb-42f8-932c-8e307467a300SPL ID b02f563b-a2cb-42f8-932c-8e307467a300SPL set ID 03efd618-8ca3-43d0-bbeb-55e53b5308e8RxCUI 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

N471205028030 followed by a unit qualifier and the quantity

Package 71205-0280-30. 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 disorder 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 stu…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209696

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

FDA NDC Directory listings under ANDA 209696
ProductStrengthForm · routeLabelerProduct NDC
Buspirone HydrochlorideBuspirone hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-1144
BusPIRone HydrochlorideBuspirone hydrochloride 15 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-291
Buspirone HydrochlorideBuspirone hydrochloride 5 mg/1TabletOralAPNAR PHARMA LP24689-781
Buspirone HydrochlorideBuspirone hydrochloride 15 mg/1TabletOralAPNAR PHARMA LP24689-921
Buspirone HydrochlorideBuspirone hydrochloride 7.5 mg/1TabletOralAPNAR PHARMA LP24689-785
Buspirone HydrochlorideBuspirone hydrochloride 10 mg/1TabletOralAPNAR PHARMA LP24689-907
Buspirone HydrochlorideBuspirone hydrochloride 30 mg/1TabletOralAPNAR PHARMA LP24689-933

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