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Guaifenesin
Guaifenesin - 50383-063-17 - (Guaifenesin)
Drug Information of Guaifenesin
| Product NDC: | 50383-063 |
| Proprietary Name: | Guaifenesin |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guaifenesin
| Product NDC: | 50383-063 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120307 |
Package Information of Guaifenesin
| Package NDC: | 50383-063-17 |
| Package Description: | 4 TRAY in 1 CASE (50383-063-17) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-063-15) > 15 mL in 1 CUP, UNIT-DOSE |
NDC Information of Guaifenesin
| NDC Code | 50383-063-17 |
| Proprietary Name | Guaifenesin |
| Package Description | 4 TRAY in 1 CASE (50383-063-17) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-063-15) > 15 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 50383-063 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120307 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
