Product NDC: | 49349-766 |
Proprietary Name: | Parafon Forte DSC |
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: | 49349-766 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA011529 |
Marketing Category: | NDA |
Start Marketing Date: | 20121128 |
Package NDC: | 49349-766-52 |
Package Description: | 25 TABLET in 1 VIAL (49349-766-52) |
NDC Code | 49349-766-52 |
Proprietary Name | Parafon Forte DSC |
Package Description | 25 TABLET in 1 VIAL (49349-766-52) |
Product NDC | 49349-766 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | chlorzoxazone |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20121128 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | CHLORZOXAZONE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |