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Liqufruta
Liqufruta - 75939-9876-2 - (GUAIFENESIN)
Drug Information of Liqufruta
| Product NDC: | 75939-9876 |
| Proprietary Name: | Liqufruta |
| Non Proprietary Name: | GUAIFENESIN |
| Active Ingredient(s): | 50 mg/5mL & nbsp; GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Liqufruta
| Product NDC: | 75939-9876 |
| Labeler Name: | Alston Garrard & Co |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110101 |
Package Information of Liqufruta
| Package NDC: | 75939-9876-2 |
| Package Description: | 200 mL in 1 BOTTLE, PLASTIC (75939-9876-2) |
NDC Information of Liqufruta
| NDC Code | 75939-9876-2 |
| Proprietary Name | Liqufruta |
| Package Description | 200 mL in 1 BOTTLE, PLASTIC (75939-9876-2) |
| Product NDC | 75939-9876 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20110101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Alston Garrard & Co |
| Substance Name | GUAIFENESIN |
| Strength Number | 50 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
