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Hybrisil
Hybrisil - 55379-405-31 - (Methylprednisolone Acetate)
Drug Information of Hybrisil
| Product NDC: | 55379-405 |
| Proprietary Name: | Hybrisil |
| Non Proprietary Name: | Methylprednisolone Acetate |
| Active Ingredient(s): | 10 mg/g & nbsp; Methylprednisolone Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hybrisil
| Product NDC: | 55379-405 |
| Labeler Name: | BioZone Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100505 |
Package Information of Hybrisil
| Package NDC: | 55379-405-31 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (55379-405-31) > 30 g in 1 BOTTLE, PUMP (55379-405-30) |
NDC Information of Hybrisil
| NDC Code | 55379-405-31 |
| Proprietary Name | Hybrisil |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (55379-405-31) > 30 g in 1 BOTTLE, PUMP (55379-405-30) |
| Product NDC | 55379-405 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylprednisolone Acetate |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100505 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | BioZone Laboratories, Inc. |
| Substance Name | METHYLPREDNISOLONE ACETATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
