Home
>
National Drug Code (NDC)
>
Fexmid
Fexmid - 21695-830-90 - (cyclobenzaprine hydrochloride)
Drug Information of Fexmid
| Product NDC: | 21695-830 |
| 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: | 21695-830 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071611 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081101 |
Package Information of Fexmid
| Package NDC: | 21695-830-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (21695-830-90) |
NDC Information of Fexmid
| NDC Code | 21695-830-90 |
| Proprietary Name | Fexmid |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (21695-830-90) |
| Product NDC | 21695-830 |
| 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 | Rebel Distributors Corp |
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
