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Guaifenesin
Guaifenesin - 55154-9425-5 - (Guaifenesin)
Drug Information of Guaifenesin
| Product NDC: | 55154-9425 |
| Proprietary Name: | Guaifenesin |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 200 mg/10mL & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guaifenesin
| Product NDC: | 55154-9425 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110602 |
Package Information of Guaifenesin
| Package NDC: | 55154-9425-5 |
| Package Description: | 5 CUP in 1 BAG (55154-9425-5) > 10 mL in 1 CUP |
NDC Information of Guaifenesin
| NDC Code | 55154-9425-5 |
| Proprietary Name | Guaifenesin |
| Package Description | 5 CUP in 1 BAG (55154-9425-5) > 10 mL in 1 CUP |
| Product NDC | 55154-9425 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110602 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | GUAIFENESIN |
| Strength Number | 200 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes |
