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Soma
Soma - 21695-606-30 - (Carisoprodol)
Drug Information of Soma
| Product NDC: | 21695-606 |
| Proprietary Name: | Soma |
| 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) |
Labeler Information of Soma
| Product NDC: | 21695-606 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011792 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070901 |
Package Information of Soma
| Package NDC: | 21695-606-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (21695-606-30) |
NDC Information of Soma
| NDC Code | 21695-606-30 |
| Proprietary Name | Soma |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (21695-606-30) |
| Product NDC | 21695-606 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carisoprodol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070901 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CARISOPRODOL |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
