NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1014Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1014Add 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
71335-1014-17133510140130 TABLET in 1 BOTTLE (71335-1014-1)Marketed from Nov 21, 2018
71335-1014-271335101402100 TABLET in 1 BOTTLE (71335-1014-2)Marketed from Aug 9, 2024
71335-1014-37133510140320 TABLET in 1 BOTTLE (71335-1014-3)Marketed from Aug 9, 2024
71335-1014-47133510140460 TABLET in 1 BOTTLE (71335-1014-4)Marketed from Aug 9, 2024
71335-1014-57133510140590 TABLET in 1 BOTTLE (71335-1014-5)Marketed from Aug 9, 2024
71335-1014-67133510140642 TABLET in 1 BOTTLE (71335-1014-6)Marketed from Aug 9, 2024
71335-1014-77133510140715 TABLET in 1 BOTTLE (71335-1014-7)Marketed from Aug 9, 2024
71335-1014-871335101408180 TABLET in 1 BOTTLE (71335-1014-8)Marketed from Aug 9, 2024

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
Generic name (nonproprietary)
oxybutynin chloride
Active ingredients
Oxybutynin chloride — 5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209025
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 71335-1014_d8012174-1a1c-46d9-9e97-094e9462a1f4SPL ID d8012174-1a1c-46d9-9e97-094e9462a1f4SPL set ID f26e590d-956e-493b-a6ac-6056aeeaf411RxCUI 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

N471335101401 followed by a unit qualifier and the quantity

Package 71335-1014-01. 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)

INDICATIONS AND USAGE Oxybutynin Chloride is 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)

Other NDCs under ANDA 209025

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

FDA NDC Directory listings under ANDA 209025
ProductStrengthForm · routeLabelerProduct NDC
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-6638
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-431
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-490
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-531
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-679
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-734
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-7766
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-417
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-8078

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