Tolterodine Tartrate
- Product NDC
- 0093-2055
- 11-digit product format
- 000932055
- Labeler code
- 0093
- Product ID
- 0093-2055_5c48e761-a899-432a-a4d6-40b900d9eb48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tolterodine Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA Inc
- Application
- NDA020771
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2012-05-11
- Marketing end
- 0000-00-00
- Substance
- TOLTERODINE TARTRATE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record