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Guaifenesin
Guaifenesin - 67046-250-30 - (guaifenesin)
Drug Information of Guaifenesin
| Product NDC: | 67046-250 |
| 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: | 67046-250 |
| Labeler Name: | Contract Pharmacy Services-PA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101006 |
Package Information of Guaifenesin
| Package NDC: | 67046-250-30 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (67046-250-30) |
NDC Information of Guaifenesin
| NDC Code | 67046-250-30 |
| Proprietary Name | Guaifenesin |
| Package Description | 30 TABLET in 1 BLISTER PACK (67046-250-30) |
| Product NDC | 67046-250 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101006 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Contract Pharmacy Services-PA |
| Substance Name | GUAIFENESIN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
