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TIZANIDINE HYDROCHLORIDE
TIZANIDINE HYDROCHLORIDE - 68387-140-10 - (TIZANIDINE HYDROCHLORIDE)
Drug Information of TIZANIDINE HYDROCHLORIDE
| Product NDC: | 68387-140 |
| 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): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TIZANIDINE HYDROCHLORIDE
| Product NDC: | 68387-140 |
| Labeler Name: | Keltman Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076347 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050601 |
Package Information of TIZANIDINE HYDROCHLORIDE
| Package NDC: | 68387-140-10 |
| Package Description: | 10 TABLET in 1 BOTTLE, PLASTIC (68387-140-10) |
NDC Information of TIZANIDINE HYDROCHLORIDE
| NDC Code | 68387-140-10 |
| Proprietary Name | TIZANIDINE HYDROCHLORIDE |
| Package Description | 10 TABLET in 1 BOTTLE, PLASTIC (68387-140-10) |
| Product NDC | 68387-140 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TIZANIDINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050601 |
| Marketing Category Name | ANDA |
| Labeler Name | Keltman 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] |
