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COPANTO
COPANTO - 49789-020-01 - (ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, CHLORPHENIRAMINE MALEATE)
Drug Information of COPANTO
| Product NDC: | 49789-020 |
| Proprietary Name: | COPANTO |
| Non Proprietary Name: | ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, CHLORPHENIRAMINE MALEATE |
| Active Ingredient(s): | 500; 3; 30 mg/670mg; mg/670mg; mg/670mg & nbsp; ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, CHLORPHENIRAMINE MALEATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of COPANTO
| Product NDC: | 49789-020 |
| 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 COPANTO
| Package NDC: | 49789-020-01 |
| Package Description: | 670 mg in 1 BLISTER PACK (49789-020-01) |
NDC Information of COPANTO
| NDC Code | 49789-020-01 |
| Proprietary Name | COPANTO |
| Package Description | 670 mg in 1 BLISTER PACK (49789-020-01) |
| Product NDC | 49789-020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, 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; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 500; 3; 30 |
| Strength Unit | mg/670mg; mg/670mg; mg/670mg |
| Pharmaceutical Classes |
