What is NDC 58151-099?

58151-099 is the product NDC for Detrol (tolterodine tartrate), Tolterodine tartrate 2 mg/1 tablet, film coated, listed with the FDA by Viatris Specialty LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Viatris Specialty LLC, NDC labeler code 58151. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Detrol?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Detrol NDC 58151-099 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)58151-099Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58151-0099Add 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
58151-099-91	5815100999158151009991	60 TABLET, FILM COATED in 1 BOTTLE (58151-099-91)Marketed from Aug 1, 2024

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): Detrol
Generic name (nonproprietary): tolterodine tartrate
Active ingredients: Tolterodine tartrate — 2 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Viatris Specialty LLCNDC labeler code 58151
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 020771
Marketing start: Aug 1, 2024
Marketing end: Jan 31, 2027
Other FDA classes: Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers: Product ID 58151-099_f27726af-7a9b-45f4-96e0-1e90a5fdcc18SPL ID f27726af-7a9b-45f4-96e0-1e90a5fdcc18SPL set ID 41eb00d2-64e3-4ec9-8732-4bfc81b04180RxCUI 855178, 855180, 855194, 855195UNII 5T619TQR3RUPC 0358151098910, 0358151099917
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

N458151009991 followed by a unit qualifier and the quantity

Package 58151-0099-91. 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 Feb 15, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE DETROL Tablets are indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58151-099

What is NDC 58151-099?: 58151-099 is the product NDC for Detrol (tolterodine tartrate), Tolterodine tartrate 2 mg/1 tablet, film coated, listed with the FDA by Viatris Specialty LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Detrol (Tolterodine tartrate).
What is the active ingredient?: Tolterodine tartrate.
Who is the labeler?: Viatris Specialty LLC, NDC labeler code 58151. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Detrol?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Detrol (Tolterodine tartrate) NDC 58151-099