Product NDC: | 35356-570 |
Proprietary Name: | Metaxalone |
Non Proprietary Name: | Metaxalone |
Active Ingredient(s): | 800 mg/1 & nbsp; Metaxalone |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-570 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA013217 |
Marketing Category: | NDA |
Start Marketing Date: | 20111206 |
Package NDC: | 35356-570-60 |
Package Description: | 60 TABLET in 1 BOTTLE (35356-570-60) |
NDC Code | 35356-570-60 |
Proprietary Name | Metaxalone |
Package Description | 60 TABLET in 1 BOTTLE (35356-570-60) |
Product NDC | 35356-570 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metaxalone |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20111206 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | METAXALONE |
Strength Number | 800 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |