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sunmark tussin
sunmark tussin - 49348-278-37 - (Guaifenesin)
Drug Information of sunmark tussin
| Product NDC: | 49348-278 |
| Proprietary Name: | sunmark tussin |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark tussin
| Product NDC: | 49348-278 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030703 |
Package Information of sunmark tussin
| Package NDC: | 49348-278-37 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-278-37) > 236 mL in 1 BOTTLE |
NDC Information of sunmark tussin
| NDC Code | 49348-278-37 |
| Proprietary Name | sunmark tussin |
| Package Description | 1 BOTTLE in 1 CARTON (49348-278-37) > 236 mL in 1 BOTTLE |
| Product NDC | 49348-278 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20030703 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
