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Zanaflex
Zanaflex - 55289-612-20 - (tizanidine hydrochloride)
Drug Information of Zanaflex
| Product NDC: | 55289-612 |
| Proprietary Name: | Zanaflex |
| Non Proprietary Name: | tizanidine hydrochloride |
| Active Ingredient(s): | 4 mg/1 & nbsp; tizanidine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zanaflex
| Product NDC: | 55289-612 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020397 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970101 |
Package Information of Zanaflex
| Package NDC: | 55289-612-20 |
| Package Description: | 20 TABLET in 1 BOTTLE, PLASTIC (55289-612-20) |
NDC Information of Zanaflex
| NDC Code | 55289-612-20 |
| Proprietary Name | Zanaflex |
| Package Description | 20 TABLET in 1 BOTTLE, PLASTIC (55289-612-20) |
| Product NDC | 55289-612 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tizanidine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970101 |
| Marketing Category Name | NDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | TIZANIDINE HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
