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Tizanidine Hydrochloride
Tizanidine Hydrochloride - 60505-2649-0 - (Tizanidine Hydrochloride)
Drug Information of Tizanidine Hydrochloride
| Product NDC: | 60505-2649 |
| Proprietary Name: | Tizanidine Hydrochloride |
| 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 Tizanidine Hydrochloride
| Product NDC: | 60505-2649 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078868 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120206 |
Package Information of Tizanidine Hydrochloride
| Package NDC: | 60505-2649-0 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (60505-2649-0) > 10 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
NDC Information of Tizanidine Hydrochloride
| NDC Code | 60505-2649-0 |
| Proprietary Name | Tizanidine Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 CARTON (60505-2649-0) > 10 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
| Product NDC | 60505-2649 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tizanidine Hydrochloride |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120206 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | TIZANIDINE HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
