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Detrol LA
Detrol LA - 0009-5191-03 - (tolterodine tartrate)
Drug Information of Detrol LA
| Product NDC: | 0009-5191 |
| Proprietary Name: | Detrol LA |
| Non Proprietary Name: | tolterodine tartrate |
| Active Ingredient(s): | 4 mg/1 & nbsp; tolterodine tartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Detrol LA
| Product NDC: | 0009-5191 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021228 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000222 |
Package Information of Detrol LA
| Package NDC: | 0009-5191-03 |
| Package Description: | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5191-03) |
NDC Information of Detrol LA
| NDC Code | 0009-5191-03 |
| Proprietary Name | Detrol LA |
| Package Description | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5191-03) |
| Product NDC | 0009-5191 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tolterodine tartrate |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20000222 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | TOLTERODINE TARTRATE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
