Product NDC: | 51525-5901 |
Proprietary Name: | Carisoprodol |
Non Proprietary Name: | carisoprodol |
Active Ingredient(s): | 250 mg/1 & nbsp; carisoprodol |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51525-5901 |
Labeler Name: | Wallace Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA011792 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20100701 |
Package NDC: | 51525-5901-1 |
Package Description: | 100 TABLET in 1 BOTTLE (51525-5901-1) |
NDC Code | 51525-5901-1 |
Proprietary Name | Carisoprodol |
Package Description | 100 TABLET in 1 BOTTLE (51525-5901-1) |
Product NDC | 51525-5901 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | carisoprodol |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100701 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Wallace Pharmaceuticals Inc. |
Substance Name | CARISOPRODOL |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |