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NDC 42806-0058-10 Flavoxate Hydrochloride 100 mg/1 Details
Flavoxate Hydrochloride 100 mg/1
Flavoxate Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Epic Pharma, LLC. The primary component is FLAVOXATE HYDROCHLORIDE.
MedlinePlus Drug Summary
Flavoxate is used to treat overactive bladder (a condition in which the bladder muscles contract uncontrollably and cause frequent urination, urgent need to urinate, and inability to control urination) relieve painful, frequent, or nighttime urination and urgency that may occur with infections of the prostate, bladder, or kidneys. Flavoxate is in a class of medications called antimuscarinics. It works by relaxing the bladder muscles. However, flavoxate is not an antibiotic; it does not cure infections.
Related Packages: 42806-0058-10Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Flavoxate
Product Information
| NDC | 42806-0058 |
|---|---|
| Product ID | 42806-058_6aeb8856-3df7-40a7-b03e-d855a58c8fa4 |
| Associated GPIs | 54400025100310 |
| GCN Sequence Number | 004927 |
| GCN Sequence Number Description | flavoxate HCl TABLET 100 MG ORAL |
| HIC3 | R1A |
| HIC3 Description | URINARY TRACT ANTISPASMODIC/ANTIINCONTINENCE AGENT |
| GCN | 19360 |
| HICL Sequence Number | 002047 |
| HICL Sequence Number Description | FLAVOXATE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Flavoxate Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Flavoxate Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 100 |
| Active Ingredient Units | mg/1 |
| Substance Name | FLAVOXATE HYDROCHLORIDE |
| Labeler Name | Epic Pharma, LLC |
| Pharmaceutical Class | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076835 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 42806-0058-10 (42806005810)
| NDC Package Code | 42806-058-10 |
|---|---|
| Billing NDC | 42806005810 |
| Package | 1000 TABLET in 1 BOTTLE (42806-058-10) |
| Marketing Start Date | 2011-02-21 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |