NDC 24658-720
Flavoxate Hydrochloride
Flavoxate Hydrochloride
Flavoxate Hydrochloride is a Oral Tablet in the Human Prescription Drug category.  It is labeled and distributed by Puracap Laboratories Llc Dba Blu Pharmaceuticals. The primary component is Flavoxate Hydrochloride.
| Product ID | 24658-720_7ea9c3f3-dcb0-7d52-e053-2a91aa0ac29a | 
| NDC | 24658-720 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Flavoxate Hydrochloride | 
| Generic Name | Flavoxate Hydrochloride | 
| Dosage Form | Tablet | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2016-12-15 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA076835 | 
| Labeler Name | PuraCap Laboratories LLC dba Blu Pharmaceuticals | 
| 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 |