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Zanaflex
Zanaflex - 21695-373-30 - (tizanidine hydrochloride)
Drug Information of Zanaflex
| Product NDC: | 21695-373 |
| Proprietary Name: | Zanaflex |
| Non Proprietary Name: | tizanidine hydrochloride |
| Active Ingredient(s): | 4 mg/1 & nbsp; tizanidine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zanaflex
| Product NDC: | 21695-373 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021447 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020829 |
Package Information of Zanaflex
| Package NDC: | 21695-373-30 |
| Package Description: | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (21695-373-30) |
NDC Information of Zanaflex
| NDC Code | 21695-373-30 |
| Proprietary Name | Zanaflex |
| Package Description | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (21695-373-30) |
| Product NDC | 21695-373 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tizanidine hydrochloride |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020829 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | TIZANIDINE HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
