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PANTO A
PANTO A - 49789-040-01 - (ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, GUAIFENESIN)
Drug Information of PANTO A
| Product NDC: | 49789-040 |
| Proprietary Name: | PANTO A |
| Non Proprietary Name: | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, GUAIFENESIN |
| Active Ingredient(s): | 300; 2.5; 83.3 mg/30mL; mg/30mL; mg/30mL & nbsp; ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PANTO A
| Product NDC: | 49789-040 |
| 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 PANTO A
| Package NDC: | 49789-040-01 |
| Package Description: | 30 mL in 1 BOTTLE (49789-040-01) |
NDC Information of PANTO A
| NDC Code | 49789-040-01 |
| Proprietary Name | PANTO A |
| Package Description | 30 mL in 1 BOTTLE (49789-040-01) |
| Product NDC | 49789-040 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, GUAIFENESIN |
| Dosage Form Name | LIQUID |
| 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; GUAIFENESIN |
| Strength Number | 300; 2.5; 83.3 |
| Strength Unit | mg/30mL; mg/30mL; mg/30mL |
| Pharmaceutical Classes |
