NDC codes

FDA NDC Directory
Product NDC (as listed)71610-860Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0860Add 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
71610-860-30716100860307161008603030 TABLET in 1 BOTTLE (71610-860-30)Marketed from Oct 10, 2024
71610-860-53716100860537161008605360 TABLET in 1 BOTTLE (71610-860-53)Marketed from Oct 10, 2024
71610-860-60716100860607161008606090 TABLET in 1 BOTTLE (71610-860-60)Marketed from Oct 10, 2024
71610-860-807161008608071610086080180 TABLET in 1 BOTTLE (71610-860-80)Marketed from Oct 10, 2024

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)
Oxybutynin Chloride
Generic name (nonproprietary)
oxybutynin chloride
Active ingredients
Oxybutynin chloride — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Aphena Pharma Solutions - Tennessee, LLCNDC labeler code 71610
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075079
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 71610-860_2425de26-9d88-2a5d-e063-6294a90acaa1SPL ID 2425de26-9d88-2a5d-e063-6294a90acaa1SPL set ID 2425f49f-ade3-5178-e063-6294a90adfacRxCUI 863664UNII L9F3D9RENQ
Pharmacologic class
Cholinergic Muscarinic Antagonist

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

N471610086030 followed by a unit qualifier and the quantity

Package 71610-0860-30. 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 Oxybutynin chloride tablets are indicated for the relief of symptoms of bladder instability associated with voiding in patients with uninhibited neurogenic or reflex neurogenic bladder (i.e., urgency, frequency, urinary leakage, urge incontinence, dysuria).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71610-860

What is NDC 71610-860?
71610-860 is the product NDC for Oxybutynin Chloride, Oxybutynin chloride 5 mg/1 tablet, listed with the FDA by Aphena Pharma Solutions - Tennessee, LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Oxybutynin Chloride.
What is the active ingredient?
Oxybutynin chloride.
Who is the labeler?
Aphena Pharma Solutions - Tennessee, LLC, NDC labeler code 71610. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oxybutynin Chloride?
79 other product NDCs are listed under this name. See all Oxybutynin Chloride 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 Oxybutynin Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralTruPharma LLC52817-26152817-0261-10
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-73464980-0734-01
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralCoupler LLC67046-138167046-1381-03
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-91323155-0913-0123155-0913-0523155-0913-10
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-67964980-0679-0164980-0679-1064980-0679-50
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-807850090-8078-0050090-8078-0150090-8078-03
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralAmerican Health Packaging60687-89960687-0899-01
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralStrides Pharma Science Limited64380-19064380-0190-01
Oxybutynin ChlorideOxybutynin chloride 15 mg/1Tablet, Extended releaseOralCoupler LLC67046-160067046-1600-03
Oxybutynin ChlorideOxybutynin chloride 5 mg/1Tablet, Extended releaseOralCoupler LLC67046-159967046-1599-03

All 80 Oxybutynin Chloride NDCs

Other NDCs under ANDA 075079

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

FDA NDC Directory listings under ANDA 075079
ProductStrengthForm · routeLabelerProduct NDC
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralStrides Pharma Science Limited64380-162
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralStrides Pharma Science Limited64380-190

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