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Stona
Stona - 49873-301-01 - (dextromethorphan hydrobromide)
Drug Information of Stona
| Product NDC: | 49873-301 |
| Proprietary Name: | Stona |
| Non Proprietary Name: | dextromethorphan hydrobromide |
| Active Ingredient(s): | 10 mg/1 & nbsp; dextromethorphan hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Stona
| Product NDC: | 49873-301 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19951119 |
Package Information of Stona
| Package NDC: | 49873-301-01 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (49873-301-01) > 12 LOZENGE in 1 BLISTER PACK |
NDC Information of Stona
| NDC Code | 49873-301-01 |
| Proprietary Name | Stona |
| Package Description | 1 BLISTER PACK in 1 CARTON (49873-301-01) > 12 LOZENGE in 1 BLISTER PACK |
| Product NDC | 49873-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan hydrobromide |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 19951119 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
