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Sucrets - 63736-850-18 - (Dyclonine Hydrochloride)
Drug Information of Sucrets
| Product NDC: | 63736-850 |
| Proprietary Name: | Sucrets |
| Non Proprietary Name: | Dyclonine Hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Dyclonine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sucrets
| Product NDC: | 63736-850 |
| Labeler Name: | Insight Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090728 |
Package Information of Sucrets
| Package NDC: | 63736-850-18 |
| Package Description: | 18 LOZENGE in 1 BOX (63736-850-18) |
NDC Information of Sucrets
| NDC Code | 63736-850-18 |
| Proprietary Name | Sucrets |
| Package Description | 18 LOZENGE in 1 BOX (63736-850-18) |
| Product NDC | 63736-850 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dyclonine Hydrochloride |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20090728 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Insight Pharmaceuticals LLC |
| Substance Name | DYCLONINE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
