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Stona
Stona - 49873-114-01 - (acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride)
Drug Information of Stona
| Product NDC: | 49873-114 |
| Proprietary Name: | Stona |
| Non Proprietary Name: | acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride |
| Active Ingredient(s): | 162.5; 2; 10; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Stona
| Product NDC: | 49873-114 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040929 |
Package Information of Stona
| Package NDC: | 49873-114-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (49873-114-01) > 24 TABLET in 1 BOTTLE |
NDC Information of Stona
| NDC Code | 49873-114-01 |
| Proprietary Name | Stona |
| Package Description | 1 BOTTLE in 1 CARTON (49873-114-01) > 24 TABLET in 1 BOTTLE |
| Product NDC | 49873-114 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040929 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 162.5; 2; 10; 5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
