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Guaifenesin
Guaifenesin - 16571-302-16 - (Guaifenesin and Codeine Phosphate)
Drug Information of Guaifenesin
| Product NDC: | 16571-302 |
| Proprietary Name: | Guaifenesin |
| 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): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guaifenesin
| Product NDC: | 16571-302 |
| Labeler Name: | Pack Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090922 |
Package Information of Guaifenesin
| Package NDC: | 16571-302-16 |
| Package Description: | 473 mL in 1 BOTTLE (16571-302-16) |
NDC Information of Guaifenesin
| NDC Code | 16571-302-16 |
| Proprietary Name | Guaifenesin |
| Package Description | 473 mL in 1 BOTTLE (16571-302-16) |
| Product NDC | 16571-302 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin and Codeine Phosphate |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20090922 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pack Pharmaceuticals LLC |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
