NDC 0574-0115
FLAVOXATE HYDROCHLORIDE
Flavoxate Hydrochloride
FLAVOXATE HYDROCHLORIDE is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Paddock Laboratories, Llc. The primary component is Flavoxate Hydrochloride.
| Product ID | 0574-0115_02549320-c5dd-4ee7-b77a-8e0904ad0394 |
| NDC | 0574-0115 |
| Product Type | Human Prescription Drug |
| Proprietary Name | FLAVOXATE HYDROCHLORIDE |
| Generic Name | Flavoxate Hydrochloride |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2004-12-22 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076831 |
| Labeler Name | Paddock Laboratories, LLC |
| Substance Name | FLAVOXATE HYDROCHLORIDE |
| Active Ingredient Strength | 100 mg/1 |
| Pharm Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |