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Fexmid
Fexmid - 68453-950-10 - (cyclobenzaprine hydrochloride)
Drug Information of Fexmid
| Product NDC: | 68453-950 |
| Proprietary Name: | Fexmid |
| Non Proprietary Name: | cyclobenzaprine hydrochloride |
| Active Ingredient(s): | 7.5 mg/1 & nbsp; cyclobenzaprine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fexmid
| Product NDC: | 68453-950 |
| Labeler Name: | Victory Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071611 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081101 |
Package Information of Fexmid
| Package NDC: | 68453-950-10 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (68453-950-10) |
NDC Information of Fexmid
| NDC Code | 68453-950-10 |
| Proprietary Name | Fexmid |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (68453-950-10) |
| Product NDC | 68453-950 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cyclobenzaprine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20081101 |
| Marketing Category Name | ANDA |
| Labeler Name | Victory Pharma, Inc. |
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
