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CHLORZOXAZONE
CHLORZOXAZONE - 16590-478-71 - (CHLORZOXAZONE)
Drug Information of CHLORZOXAZONE
| Product NDC: | 16590-478 |
| Proprietary Name: | CHLORZOXAZONE |
| Non Proprietary Name: | CHLORZOXAZONE |
| Active Ingredient(s): | 500 mg/1 & nbsp; CHLORZOXAZONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CHLORZOXAZONE
| Product NDC: | 16590-478 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089859 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081223 |
Package Information of CHLORZOXAZONE
| Package NDC: | 16590-478-71 |
| Package Description: | 100 TABLET in 1 BOTTLE (16590-478-71) |
NDC Information of CHLORZOXAZONE
| NDC Code | 16590-478-71 |
| Proprietary Name | CHLORZOXAZONE |
| Package Description | 100 TABLET in 1 BOTTLE (16590-478-71) |
| Product NDC | 16590-478 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLORZOXAZONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081223 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | CHLORZOXAZONE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
