| Product NDC: | 0603-4886 |
| Proprietary Name: | ORGAN-I NR |
| Non Proprietary Name: | guaifenesin |
| Active Ingredient(s): | 200 mg/1 & nbsp; guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0603-4886 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20020701 |
| Package NDC: | 0603-4886-21 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0603-4886-21) |
| NDC Code | 0603-4886-21 |
| Proprietary Name | ORGAN-I NR |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0603-4886-21) |
| Product NDC | 0603-4886 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | GUAIFENESIN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |