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Pandel
Pandel - 0462-0153-46 - (Hydrocortisone Probutate)
Drug Information of Pandel
| Product NDC: | 0462-0153 |
| Proprietary Name: | Pandel |
| Non Proprietary Name: | Hydrocortisone Probutate |
| Active Ingredient(s): | 1 mg/g & nbsp; Hydrocortisone Probutate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pandel
| Product NDC: | 0462-0153 |
| Labeler Name: | PharmaDerm, A division of Nycomed US Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020453 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970228 |
Package Information of Pandel
| Package NDC: | 0462-0153-46 |
| Package Description: | 45 g in 1 TUBE (0462-0153-46) |
NDC Information of Pandel
| NDC Code | 0462-0153-46 |
| Proprietary Name | Pandel |
| Package Description | 45 g in 1 TUBE (0462-0153-46) |
| Product NDC | 0462-0153 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Probutate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19970228 |
| Marketing Category Name | NDA |
| Labeler Name | PharmaDerm, A division of Nycomed US Inc. |
| Substance Name | HYDROCORTISONE PROBUTATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
