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MUCOSA
MUCOSA - 49483-272-06 - (GUAIFENESIN)
Drug Information of MUCOSA
| Product NDC: | 49483-272 |
| Proprietary Name: | MUCOSA |
| 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) |
Labeler Information of MUCOSA
| Product NDC: | 49483-272 |
| Labeler Name: | TIME CAP LABORATORIES, INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120416 |
Package Information of MUCOSA
| Package NDC: | 49483-272-06 |
| Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (49483-272-06) |
NDC Information of MUCOSA
| NDC Code | 49483-272-06 |
| Proprietary Name | MUCOSA |
| Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (49483-272-06) |
| Product NDC | 49483-272 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120416 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TIME CAP LABORATORIES, INC |
| Substance Name | GUAIFENESIN |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
