Product NDC: | 59800-0232 |
Proprietary Name: | Air Power |
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) |
Product NDC: | 59800-0232 |
Labeler Name: | Enzymatic Therapy, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20030519 |
Package NDC: | 59800-0232-1 |
Package Description: | 100 TABLET in 1 BOTTLE (59800-0232-1) |
NDC Code | 59800-0232-1 |
Proprietary Name | Air Power |
Package Description | 100 TABLET in 1 BOTTLE (59800-0232-1) |
Product NDC | 59800-0232 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | GUAIFENESIN |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20030519 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Enzymatic Therapy, Inc. |
Substance Name | GUAIFENESIN |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |