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PANDEL
PANDEL - 10337-153-46 - (HYDROCORTISONE PROBUTATE)
Drug Information of PANDEL
| Product NDC: | 10337-153 |
| 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: | 10337-153 |
| Labeler Name: | PharmaDerm a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020453 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970228 |
Package Information of PANDEL
| Package NDC: | 10337-153-46 |
| Package Description: | 1 TUBE in 1 CARTON (10337-153-46) > 45 g in 1 TUBE |
NDC Information of PANDEL
| NDC Code | 10337-153-46 |
| Proprietary Name | PANDEL |
| Package Description | 1 TUBE in 1 CARTON (10337-153-46) > 45 g in 1 TUBE |
| Product NDC | 10337-153 |
| 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 Fougera Pharmaceuticals Inc. |
| Substance Name | HYDROCORTISONE PROBUTATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
