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Guaifenesin
Guaifenesin - 0904-5154-60 - (Guaifenesin)
Drug Information of Guaifenesin
| Product NDC: | 0904-5154 |
| Proprietary Name: | Guaifenesin |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 200 mg/1 & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guaifenesin
| Product NDC: | 0904-5154 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091005 |
Package Information of Guaifenesin
| Package NDC: | 0904-5154-60 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0904-5154-60) > 100 TABLET in 1 BOTTLE, PLASTIC |
NDC Information of Guaifenesin
| NDC Code | 0904-5154-60 |
| Proprietary Name | Guaifenesin |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0904-5154-60) > 100 TABLET in 1 BOTTLE, PLASTIC |
| Product NDC | 0904-5154 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091005 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | GUAIFENESIN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
