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Kondremul
Kondremul - 63736-012-16 - (Kondremul)
Drug Information of Kondremul
| Product NDC: | 63736-012 |
| Proprietary Name: | Kondremul |
| Non Proprietary Name: | Kondremul |
| Active Ingredient(s): | 2.5 mL/5mL & nbsp; Kondremul |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kondremul
| Product NDC: | 63736-012 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090605 |
Package Information of Kondremul
| Package NDC: | 63736-012-16 |
| Package Description: | 480 mL in 1 BOTTLE (63736-012-16) |
NDC Information of Kondremul
| NDC Code | 63736-012-16 |
| Proprietary Name | Kondremul |
| Package Description | 480 mL in 1 BOTTLE (63736-012-16) |
| Product NDC | 63736-012 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Kondremul |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090605 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | MINERAL OIL |
| Strength Number | 2.5 |
| Strength Unit | mL/5mL |
| Pharmaceutical Classes |
