Product NDC: | 61787-063 |
Proprietary Name: | Diabetic Tussin Expectorant |
Non Proprietary Name: | Guaifenesin |
Active Ingredient(s): | 100 mg/5mL & nbsp; Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61787-063 |
Labeler Name: | Health Care Products |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19960101 |
Package NDC: | 61787-063-04 |
Package Description: | 1 BOTTLE in 1 BOX (61787-063-04) > 118 mL in 1 BOTTLE |
NDC Code | 61787-063-04 |
Proprietary Name | Diabetic Tussin Expectorant |
Package Description | 1 BOTTLE in 1 BOX (61787-063-04) > 118 mL in 1 BOTTLE |
Product NDC | 61787-063 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19960101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Health Care Products |
Substance Name | GUAIFENESIN |
Strength Number | 100 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |