NDC codes

FDA NDC Directory
Product NDC (as listed)27241-191Labeler and product segments. Claims need a package NDC.
Product NDC at billing width27241-0191Add 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
27241-191-052724101910527241019105500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (27241-191-05)Marketed from Jun 25, 2020
27241-191-30272410191302724101913030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (27241-191-30)Marketed from Jun 25, 2020
27241-191-90272410191902724101919090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (27241-191-90)Marketed from Jun 25, 2020

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)
Tolterodine tartrate
Generic name (nonproprietary)
tolterodine tartrate
Active ingredients
Tolterodine tartrate — 2 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Labeler
Ajanta Pharma USA Inc.NDC labeler code 27241
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213397
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 27241-191_cf018a04-660f-4119-898f-1877a5db8e7eSPL ID cf018a04-660f-4119-898f-1877a5db8e7eSPL set ID fcaca033-cd08-4b8c-9bad-7b6751faf2c9RxCUI 855182, 855189UNII 5T619TQR3RUPC 0327241192302, 0327241191305
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

N427241019105 followed by a unit qualifier and the quantity

Package 27241-0191-05. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 27241-191

What is NDC 27241-191?
27241-191 is the product NDC for Tolterodine tartrate, Tolterodine tartrate 2 mg/1 capsule, extended release, listed with the FDA by Ajanta Pharma USA Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Tolterodine tartrate.
What is the active ingredient?
Tolterodine tartrate.
Who is the labeler?
Ajanta Pharma USA Inc., NDC labeler code 27241. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Tolterodine tartrate?
31 other product NDCs are listed under this name. See all Tolterodine tartrate 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 Tolterodine tartrate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Tolterodine TartrateTolterodine tartrate 2 mg/1Capsule, Extended releaseOralMajor Pharmaceuticals0904-757400904-7574-04
Tolterodine TartrateTolterodine tartrate 4 mg/1Capsule, Extended releaseOralMajor Pharmaceuticals0904-757500904-7575-04
Tolterodine tartrateTolterodine tartrate 4 mg/1Capsule, Extended releaseOralUnichem Pharmaceuticals (USA), Inc.29300-30729300-0307-0529300-0307-1329300-0307-19
Tolterodine tartrateTolterodine tartrate 2 mg/1Capsule, Extended releaseOralUnichem Pharmaceuticals (USA), Inc.29300-30629300-0306-0529300-0306-1329300-0306-19
Tolterodine TartrateTolterodine tartrate 2 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-80631722-0806-0131722-0806-0231722-0806-05+1 more
Tolterodine TartrateTolterodine tartrate 1 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-80531722-0805-0131722-0805-0231722-0805-05+1 more
Tolterodine TartrateTolterodine tartrate 2 mg/1Capsule, Extended releaseOralSlate Run Pharmaceuticals, LLC70436-16070436-0160-0270436-0160-0470436-0160-06
Tolterodine TartrateTolterodine tartrate 4 mg/1Capsule, Extended releaseOralSlate Run Pharmaceuticals, LLC70436-16170436-0161-0270436-0161-0470436-0161-06
Tolterodine tartrateTolterodine tartrate 2 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-09833342-0098-0933342-0098-1233342-0098-15
Tolterodine tartrateTolterodine tartrate 1 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-09733342-0097-0933342-0097-1233342-0097-15

All 32 Tolterodine tartrate NDCs

Other NDCs under ANDA 213397

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

FDA NDC Directory listings under ANDA 213397
ProductStrengthForm · routeLabelerProduct NDC
Tolterodine tartrateTolterodine tartrate 4 mg/1Capsule, Extended releaseOralAjanta Pharma USA Inc.27241-192

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