Tolterodine Tartrate NDC 0093-7163

NDC codes

FDA NDC Directory

Product NDC (as listed)0093-7163Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00093-7163Add 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
0093-7163-05	00093716305	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7163-05)Marketed from Mar 20, 2017
0093-7163-56	00093716356	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7163-56)Marketed from Mar 20, 2017
0093-7163-98	00093716398	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7163-98)Marketed from Mar 20, 2017

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Tolterodine Tartrate
Generic name (nonproprietary): tolterodine tartrate
Active ingredients: Tolterodine tartrate — 2 mg/1
Dosage form: Capsule, Extended release
Route: Oral
Labeler: Teva Pharmaceuticals USA, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 079141
Marketing start: Mar 20, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers: Product ID 0093-7163_acae7de6-a2b9-4475-8b25-620c0fa55235SPL ID acae7de6-a2b9-4475-8b25-620c0fa55235SPL set ID 973f98b5-4e8a-42d9-ac69-d4333d21c362RxCUI 855182, 855189UNII 5T619TQR3RUPC 0300937164562, 0300937163565
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

N400093716305 followed by a unit qualifier and the quantity

Package 00093-7163-05. 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 Sep 25, 2024.

Indications (excerpt from the label)

Tolterodine tartrate extended-release capsules are indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency [ see CLINICAL STUDIES ( 14 ) ]. Tolterodine tartrate extended-release capsules are an antimuscarinic indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 079141

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

FDA NDC Directory listings under ANDA 079141
Product	Strength	Form · route	Labeler	Product NDC
Tolterodine Tartrate	Tolterodine tartrate 4 mg/1	Capsule, Extended releaseOral	Teva Pharmaceuticals USA, Inc.	0093-7164
Tolterodine Tartrate	Tolterodine tartrate 4 mg/1	Capsule, Extended releaseOral	A-S Medication Solutions	50090-3475