| Product NDC: | 54569-3403 |
| Proprietary Name: | Carisoprodol |
| Non Proprietary Name: | Carisoprodol |
| Active Ingredient(s): | 350 mg/1 & nbsp; Carisoprodol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54569-3403 |
| Labeler Name: | A-S Medication Solutions LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040245 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970908 |
| Package NDC: | 54569-3403-5 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (54569-3403-5) |
| NDC Code | 54569-3403-5 |
| Proprietary Name | Carisoprodol |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (54569-3403-5) |
| Product NDC | 54569-3403 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carisoprodol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970908 |
| Marketing Category Name | ANDA |
| Labeler Name | A-S Medication Solutions LLC |
| Substance Name | CARISOPRODOL |
| Strength Number | 350 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |