What is NDC 71205-667?

71205-667 is the product NDC for oxybutynin chloride, Oxybutynin chloride 10 mg/1 tablet, extended release, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

oxybutynin chloride NDC 71205-667 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-667Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0667Add 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 NDC	11-digit (billing)	Package
71205-667-30	7120506673071205066730	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-30)Marketed from Jun 8, 2022
71205-667-60	7120506676071205066760	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-60)Marketed from Jun 8, 2022
71205-667-90	7120506679071205066790	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)Marketed from Jun 8, 2022

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 — 10 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207138
Marketing start: Dec 20, 2016
Listing expires: Dec 31, 2027
Other FDA classes: Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers: Product ID 71205-667_88f08450-559e-4038-aad1-051e4ab283cfSPL ID 88f08450-559e-4038-aad1-051e4ab283cfSPL set ID 88f08450-559e-4038-aad1-051e4ab283cfRxCUI 863619UNII L9F3D9RENQUPC 0371205667306
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

N471205066730 followed by a unit qualifier and the quantity

Package 71205-0667-30. 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 Jun 1, 2022.

Indications (excerpt from the label)

Oxybutynin chloride extended-release tablets are 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. ( Error! Hyperlink reference not valid. ) • Oxybutynin chloride extended-release tablets …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-667

What is NDC 71205-667?: 71205-667 is the product NDC for oxybutynin chloride, Oxybutynin chloride 10 mg/1 tablet, extended release, listed with the FDA by Proficient Rx LP. It has 3 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?: Proficient Rx LP, NDC labeler code 71205. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Oxybutynin Chloride	Oxybutynin chloride 2.5 mg/1	TabletOral	TruPharma LLC	52817-261	52817-0261-10
Oxybutynin Chloride	Oxybutynin chloride 2.5 mg/1	TabletOral	RISING PHARMA HOLDINGS, INC.	64980-734	64980-0734-01
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	Coupler LLC	67046-1381	67046-1381-03
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-913	23155-0913-0123155-0913-0523155-0913-10
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	RISING PHARMA HOLDINGS, INC.	64980-679	64980-0679-0164980-0679-1064980-0679-50
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	A-S Medication Solutions	50090-8078	50090-8078-0050090-8078-0150090-8078-03
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	American Health Packaging	60687-899	60687-0899-01
Oxybutynin Chloride	Oxybutynin chloride 2.5 mg/1	TabletOral	Strides Pharma Science Limited	64380-190	64380-0190-01
Oxybutynin Chloride	Oxybutynin chloride 15 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1600	67046-1600-03
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1599	67046-1599-03

All 80 oxybutynin chloride NDCs

Other NDCs under ANDA 207138

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

FDA NDC Directory listings under ANDA 207138
Product	Strength	Form · route	Labeler	Product NDC
oxybutynin chloride	Oxybutynin chloride 5 mg/1	Tablet, Extended releaseOral	Accord Healthcare, Inc.	16729-317
oxybutynin chloride	Oxybutynin chloride 10 mg/1	Tablet, Extended releaseOral	Accord Healthcare, Inc.	16729-318
oxybutynin chloride	Oxybutynin chloride 15 mg/1	Tablet, Extended releaseOral	Accord Healthcare, Inc.	16729-319
oxybutynin chloride	Oxybutynin chloride 10 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-4307
oxybutynin chloride	Oxybutynin chloride 5 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-5822
oxybutynin chloride	Oxybutynin chloride 5 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	63629-9689
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	Tablet, Extended releaseOral	direct rx	72189-131
Oxybutynin Chloride	Oxybutynin chloride 10 mg/1	Tablet, Extended releaseOral	DIRECT RX	72189-132
oxybutynin chloride	Oxybutynin chloride 10 mg/1	Tablet, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-049