NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2121Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2121Add 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
71335-2121-17133521210130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-1)Marketed from Jun 20, 2022
71335-2121-27133521210218 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-2)Marketed from Jun 20, 2022
71335-2121-37133521210390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-3)Marketed from Jun 20, 2022
71335-2121-47133521210460 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2121-4)Marketed from Jun 20, 2022

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)
Oxybutynin Chloride Extended ReleaseSuffix: Extended Release
Generic name (nonproprietary)
oxybutynin chloride
Active ingredients
Oxybutynin chloride — 10 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206121
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 71335-2121_9b4a7465-5a1a-4474-b2d3-9befee70bc1cSPL ID 9b4a7465-5a1a-4474-b2d3-9befee70bc1cSPL set ID 169d6d58-8887-4bdd-95bd-873d1f049eaaRxCUI 863619UNII 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

N471335212101 followed by a unit qualifier and the quantity

Package 71335-2121-01. 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)

Oxybutynin chloride extended-release tablets are a muscarinic antagonist indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency. Oxybutynin chloride extended-release tablets are also indicated for the treatment of pediatric patients aged 6 years and older with symptoms of detrusor overactivity associated with a neurological condition (e.g., spina bifida). Oxybutynin chloride extended-release tablets are a muscarinic antagonist indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency. ( 1 ) Oxybutynin chloride extended-release tablets are also indicated for the treatment o…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 206121

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

FDA NDC Directory listings under ANDA 206121
ProductStrengthForm · routeLabelerProduct NDC
Oxybutynin Chloride Extended Releaseoxybutynin chlorideOxybutynin chloride 5 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2330
Oxybutynin Chloride Extended Releaseoxybutynin chlorideOxybutynin chloride 10 mg/1Tablet, Extended releaseOralProficient Rx LP82804-095
Oxybutynin Chloride Extended Releaseoxybutynin chlorideOxybutynin chloride 10 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6673
Oxybutynin Chloride Extended Releaseoxybutynin chlorideOxybutynin chloride 5 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6840
Oxybutynin Chloride Extended Releaseoxybutynin chlorideOxybutynin chloride 5 mg/1Tablet, Extended releaseOralRising Pharma Holdings, Inc.64980-209
Oxybutynin Chloride Extended Releaseoxybutynin chlorideOxybutynin chloride 10 mg/1Tablet, Extended releaseOralRising Pharma Holdings, Inc.64980-210
Oxybutynin Chloride Extended Releaseoxybutynin chlorideOxybutynin chloride 10 mg/1Tablet, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-414
Oxybutynin Chloride Extended Releaseoxybutynin chlorideOxybutynin chloride 15 mg/1Tablet, Extended releaseOralRising Pharma Holdings, Inc.64980-211

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