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Detrol
Detrol - 0009-4541-02 - (tolterodine tartrate)
Drug Information of Detrol
| Product NDC: | 0009-4541 |
| Proprietary Name: | Detrol |
| Non Proprietary Name: | tolterodine tartrate |
| Active Ingredient(s): | 1 mg/1 & nbsp; tolterodine tartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Detrol
| Product NDC: | 0009-4541 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020771 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980325 |
Package Information of Detrol
| Package NDC: | 0009-4541-02 |
| Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (0009-4541-02) |
NDC Information of Detrol
| NDC Code | 0009-4541-02 |
| Proprietary Name | Detrol |
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (0009-4541-02) |
| Product NDC | 0009-4541 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tolterodine tartrate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19980325 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | TOLTERODINE TARTRATE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
