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Guaiatussin AC
Guaiatussin AC - 50383-087-04 - (guaifenesin and codeine phosphate)
Drug Information of Guaiatussin AC
| Product NDC: | 50383-087 |
| Proprietary Name: | Guaiatussin AC |
| Non Proprietary Name: | guaifenesin and codeine phosphate |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; guaifenesin and codeine phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guaiatussin AC
| Product NDC: | 50383-087 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100908 |
Package Information of Guaiatussin AC
| Package NDC: | 50383-087-04 |
| Package Description: | 118 mL in 1 BOTTLE (50383-087-04) |
NDC Information of Guaiatussin AC
| NDC Code | 50383-087-04 |
| Proprietary Name | Guaiatussin AC |
| Package Description | 118 mL in 1 BOTTLE (50383-087-04) |
| Product NDC | 50383-087 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | guaifenesin and codeine phosphate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100908 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
