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Anusol
Anusol - 65649-401-30 - (hydrocortisone)
Drug Information of Anusol
| Product NDC: | 65649-401 |
| Proprietary Name: | Anusol |
| Non Proprietary Name: | hydrocortisone |
| Active Ingredient(s): | 25 mg/g & nbsp; hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anusol
| Product NDC: | 65649-401 |
| Labeler Name: | Salix Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088250 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19840606 |
Package Information of Anusol
| Package NDC: | 65649-401-30 |
| Package Description: | 30 g in 1 TUBE (65649-401-30) |
NDC Information of Anusol
| NDC Code | 65649-401-30 |
| Proprietary Name | Anusol |
| Package Description | 30 g in 1 TUBE (65649-401-30) |
| Product NDC | 65649-401 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19840606 |
| Marketing Category Name | ANDA |
| Labeler Name | Salix Pharmaceuticals, Inc |
| Substance Name | HYDROCORTISONE |
| Strength Number | 25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
