Tolterodine Tartrate
- Product NDC
- 59762-0170
- 11-digit product format
- 597620170
- Labeler code
- 59762
- Product ID
- 59762-0170_fdede630-529a-48fe-b796-59c3504c8d32
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tolterodine Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- NDA020771
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-01-21
- Marketing end
- 2026-08-31
- Substance
- TOLTERODINE TARTRATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tolterodine Tartrate
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLTERODINE TARTRATE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5T619TQR3R |
| Rxcui | 855178, 855194 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59762-0170-1 | Tolterodine Tartrate | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 12 |
| 59762-0170-6 | Tolterodine Tartrate | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 12 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| TOLTERODINE TARTRATE | ACTIVE INGREDIENT | 5T619TQR3R | TOLTERODINE TARTRATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| TOLTERODINE | ACTIVE MOIETY | WHE7A56U7K | TOLTERODINE TARTRATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | TOLTERODINE TARTRATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | TOLTERODINE TARTRATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | TOLTERODINE TARTRATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | TOLTERODINE TARTRATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | TOLTERODINE TARTRATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | TOLTERODINE TARTRATE TABLET, FILM COATED [GREENSTONE LLC] | 4 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59762-0170 | TOLTERODINE TARTRATE TABLET, FILM COATED [MYLAN PHARMACEUTICALS INC.] | 11 | Current NDC, Legacy NDC, 2 package rows | 20250504_9e432622-2e6f-4cf8-892f-510288dd50f2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59762-0170-1 | 59762017001 | 500 TABLET, FILM COATED in 1 BOTTLE (59762-0170-1) | 2014-01-21 | 0000-00-00 | No | No | Current |
| 59762-0170-6 | 59762017006 | 60 TABLET, FILM COATED in 1 BOTTLE (59762-0170-6) | 2014-01-21 | 2026-08-31 | No | No | Current |