Product NDC: | 68016-019 |
Proprietary Name: | Premier Value Chest Congestion 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) |
Product NDC: | 68016-019 |
Labeler Name: | Premier Value |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090504 |
Package NDC: | 68016-019-01 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (68016-019-01) > 50 TABLET in 1 BOTTLE, PLASTIC (68016-019-65) |
NDC Code | 68016-019-01 |
Proprietary Name | Premier Value Chest Congestion Relief |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (68016-019-01) > 50 TABLET in 1 BOTTLE, PLASTIC (68016-019-65) |
Product NDC | 68016-019 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090504 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Premier Value |
Substance Name | GUAIFENESIN |
Strength Number | 400 |
Strength Unit | mg/1 |
Pharmaceutical Classes |