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Mucus Relief
Mucus Relief - 59726-107-30 - (Guaifenesin)
Drug Information of Mucus Relief
| Product NDC: | 59726-107 |
| Proprietary Name: | Mucus Relief |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 400 mg/1 & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucus Relief
| Product NDC: | 59726-107 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121207 |
Package Information of Mucus Relief
| Package NDC: | 59726-107-30 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (59726-107-30) > 30 TABLET in 1 BOTTLE, PLASTIC |
NDC Information of Mucus Relief
| NDC Code | 59726-107-30 |
| Proprietary Name | Mucus Relief |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (59726-107-30) > 30 TABLET in 1 BOTTLE, PLASTIC |
| Product NDC | 59726-107 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121207 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | GUAIFENESIN |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
