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MucaPlex
MucaPlex - 59800-7232-1 - (GUAIFENESIN)
Drug Information of MucaPlex
| Product NDC: | 59800-7232 |
| Proprietary Name: | MucaPlex |
| 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) |
Labeler Information of MucaPlex
| Product NDC: | 59800-7232 |
| Labeler Name: | Enzymatic Therapy, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20051001 |
Package Information of MucaPlex
| Package NDC: | 59800-7232-1 |
| Package Description: | 100 TABLET in 1 BOTTLE (59800-7232-1) |
NDC Information of MucaPlex
| NDC Code | 59800-7232-1 |
| Proprietary Name | MucaPlex |
| Package Description | 100 TABLET in 1 BOTTLE (59800-7232-1) |
| Product NDC | 59800-7232 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20051001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Enzymatic Therapy, Inc. |
| Substance Name | GUAIFENESIN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
