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Flavoxate Hydrochloride
Flavoxate Hydrochloride - 51224-154-70 - (Flavoxate hydrochloride)
Drug Information of Flavoxate Hydrochloride
| Product NDC: | 51224-154 |
| Proprietary Name: | Flavoxate Hydrochloride |
| Non Proprietary Name: | Flavoxate hydrochloride |
| Active Ingredient(s): | 100 mg/1 & nbsp; Flavoxate hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flavoxate Hydrochloride
| Product NDC: | 51224-154 |
| Labeler Name: | TAGI Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076835 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110325 |
Package Information of Flavoxate Hydrochloride
| Package NDC: | 51224-154-70 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (51224-154-70) |
NDC Information of Flavoxate Hydrochloride
| NDC Code | 51224-154-70 |
| Proprietary Name | Flavoxate Hydrochloride |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (51224-154-70) |
| Product NDC | 51224-154 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flavoxate hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110325 |
| Marketing Category Name | ANDA |
| Labeler Name | TAGI Pharma, Inc. |
| Substance Name | FLAVOXATE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
