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GUAAP
GUAAP - 46084-051-21 - (GUAIFENESIN)
Drug Information of GUAAP
| Product NDC: | 46084-051 |
| Proprietary Name: | GUAAP |
| Non Proprietary Name: | GUAIFENESIN |
| Active Ingredient(s): | 100 mg/5mL & nbsp; GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GUAAP
| Product NDC: | 46084-051 |
| Labeler Name: | A P J Laboratories Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130301 |
Package Information of GUAAP
| Package NDC: | 46084-051-21 |
| Package Description: | 120 mL in 1 BOTTLE (46084-051-21) |
NDC Information of GUAAP
| NDC Code | 46084-051-21 |
| Proprietary Name | GUAAP |
| Package Description | 120 mL in 1 BOTTLE (46084-051-21) |
| Product NDC | 46084-051 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | A P J Laboratories Limited |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
