Tolterodine Tartrate
- Product NDC
- 29300-239
- 11-digit product format
- 293000239
- Labeler code
- 29300
- Product ID
- 29300-239_9faf1be0-1f13-47c0-b2aa-3ad62e5037e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tolterodine Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Application
- ANDA205399
- Marketing category
- ANDA
- Marketing start
- 2020-08-05
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5T619TQR3R | TOLTERODINE TARTRATE | 124937-52-6 | TOLTERODINE TARTRATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 29300-239-05 | 29300023905 | 500 TABLET in 1 BOTTLE, PLASTIC (29300-239-05) | 500 tablet | 2020-08-05 | No | No | Historical |
| 29300-239-16 | 29300023916 | 60 TABLET in 1 BOTTLE, PLASTIC (29300-239-16) | 60 tablet | 2020-08-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tolterodine Tartrate Tablets | Unichem Pharmaceuticals (USA), Inc. | 2020-08-07 | HUMAN PRESCRIPTION DRUG LABEL | 3 |