Product NDC: | 54868-0735 |
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) |
Product NDC: | 54868-0735 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089859 |
Marketing Category: | ANDA |
Start Marketing Date: | 19950424 |
Package NDC: | 54868-0735-5 |
Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (54868-0735-5) |
NDC Code | 54868-0735-5 |
Proprietary Name | Chlorzoxazone |
Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-0735-5) |
Product NDC | 54868-0735 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Chlorzoxazone |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19950424 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | CHLORZOXAZONE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |