Tolterodine Tartrate
- Product NDC
- 0093-0010
- 11-digit product format
- 000930010
- Labeler code
- 0093
- Product ID
- 0093-0010_2f429822-d6d2-43c0-9aaf-1270b3e92a2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tolterodine Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA077006
- Marketing category
- ANDA
- Marketing start
- 2015-11-01
- Substance
- TOLTERODINE TARTRATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tolterodine Tartrate
- Listing expiration
- 2026-12-31
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 |
|---|
| 0093-0010-05 | Tolterodine Tartrate | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 4 |
| 0093-0010-06 | Tolterodine Tartrate | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 4 |
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 [TEVA PHARMACEUTICALS USA INC] | 1 | |
| TOLTERODINE | ACTIVE MOIETY | WHE7A56U7K | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
| HYPROMELLOSE 2910 (15 MPA.S) | INACTIVE INGREDIENT | 36SFW2JZ0W | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
| POLYETHYLENE GLYCOL 6000 | INACTIVE INGREDIENT | 30IQX730WE | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
| SODIUM STEARYL FUMARATE | INACTIVE INGREDIENT | 7CV7WJK4UI | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0093-0010 | TOLTERODINE TARTRATE TABLET, FILM COATED [TEVA PHARMACEUTICALS USA, INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20221019_d27e25b5-5d02-419f-b098-41fb162c5872.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 |
|---|
| 0093-0010-05 | 00093001005 | 500 in 1 BOTTLE | | | | | Historical |
| 0093-0010-06 | 00093001006 | 60 TABLET, FILM COATED in 1 BOTTLE (0093-0010-06) | 2015-11-01 | 0000-00-00 | No | No | Current |