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Liquituss GG
Liquituss GG - 64543-125-04 - (guaifenesin)
Drug Information of Liquituss GG
| Product NDC: | 64543-125 |
| Proprietary Name: | Liquituss GG |
| Non Proprietary Name: | guaifenesin |
| Active Ingredient(s): | 200 mg/5mL & nbsp; guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Liquituss GG
| Product NDC: | 64543-125 |
| Labeler Name: | Capellon Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120615 |
Package Information of Liquituss GG
| Package NDC: | 64543-125-04 |
| Package Description: | 118 mL in 1 BOTTLE (64543-125-04) |
NDC Information of Liquituss GG
| NDC Code | 64543-125-04 |
| Proprietary Name | Liquituss GG |
| Package Description | 118 mL in 1 BOTTLE (64543-125-04) |
| Product NDC | 64543-125 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120615 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Capellon Pharmaceuticals, LLC |
| Substance Name | GUAIFENESIN |
| Strength Number | 200 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
