Product NDC: | 50844-532 |
Proprietary Name: | Mucus Relief |
Non Proprietary Name: | Guaifenesin |
Active Ingredient(s): | 400 mg/1 & nbsp; Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50844-532 |
Labeler Name: | L.N.K. International, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19951222 |
Package NDC: | 50844-532-11 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (50844-532-11) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
NDC Code | 50844-532-11 |
Proprietary Name | Mucus Relief |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50844-532-11) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
Product NDC | 50844-532 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19951222 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | L.N.K. International, Inc. |
Substance Name | GUAIFENESIN |
Strength Number | 400 |
Strength Unit | mg/1 |
Pharmaceutical Classes |