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ALLPANTO S
ALLPANTO S - 49789-010-01 - (ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE)
Drug Information of ALLPANTO S
| Product NDC: | 49789-010 |
| Proprietary Name: | ALLPANTO S |
| Non Proprietary Name: | ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE |
| Active Ingredient(s): | 162.5; 1; 7.5; 15 mg/448mg; mg/448mg; mg/448mg; mg/448mg & nbsp; ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALLPANTO S
| Product NDC: | 49789-010 |
| Labeler Name: | SAMSUNG PHARM IND. CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120301 |
Package Information of ALLPANTO S
| Package NDC: | 49789-010-01 |
| Package Description: | 488 mg in 1 BLISTER PACK (49789-010-01) |
NDC Information of ALLPANTO S
| NDC Code | 49789-010-01 |
| Proprietary Name | ALLPANTO S |
| Package Description | 488 mg in 1 BLISTER PACK (49789-010-01) |
| Product NDC | 49789-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SAMSUNG PHARM IND. CO., LTD. |
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 162.5; 1; 7.5; 15 |
| Strength Unit | mg/448mg; mg/448mg; mg/448mg; mg/448mg |
| Pharmaceutical Classes |
