What is NDC 60687-899?

60687-899 is the product NDC for Oxybutynin Chloride, Oxybutynin chloride 5 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.

American Health Packaging, NDC labeler code 60687. 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 60687-899 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60687-899Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60687-0899Add 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	Copy
60687-899-01	6068708990160687089901	100 BLISTER PACK in 1 CARTON (60687-899-01) / 1 TABLET in 1 BLISTER PACK (60687-899-11)Marketed from Apr 16, 2026

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: American Health PackagingNDC labeler code 60687
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208165
Marketing start: Apr 16, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers: Product ID 60687-899_4f95e208-d97b-e807-e063-6394a90a801eSPL ID 4f95e208-d97b-e807-e063-6394a90a801eSPL set ID 4574b227-9726-4798-bac2-83bfb9616f09RxCUI 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

N460687089901 followed by a unit qualifier and the quantity

Package 60687-0899-01. 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 Apr 16, 2026.

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 60687-899

What is NDC 60687-899?: 60687-899 is the product NDC for Oxybutynin Chloride, Oxybutynin chloride 5 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, 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?: American Health Packaging, NDC labeler code 60687. 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 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
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	AvKARE	42291-456	42291-0456-50

All 80 Oxybutynin Chloride NDCs

Other NDCs under ANDA 208165

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

FDA NDC Directory listings under ANDA 208165
Product	Strength	Form · route	Labeler	Product NDC
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-810
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	AvKARE	42291-456
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	Strides Pharma Science Limited	64380-781
Oxybutynin Chloride	Oxybutynin chloride 5 mg/1	TabletOral	Coupler LLC	67046-1381