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Alacort
Alacort - 0316-0126-01 - (Hydrocortisone)
Drug Information of Alacort
| Product NDC: | 0316-0126 |
| Proprietary Name: | Alacort |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 10 mg/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alacort
| Product NDC: | 0316-0126 |
| Labeler Name: | Crown Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080706 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19730309 |
Package Information of Alacort
| Package NDC: | 0316-0126-01 |
| Package Description: | 28.4 g in 1 TUBE (0316-0126-01) |
NDC Information of Alacort
| NDC Code | 0316-0126-01 |
| Proprietary Name | Alacort |
| Package Description | 28.4 g in 1 TUBE (0316-0126-01) |
| Product NDC | 0316-0126 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19730309 |
| Marketing Category Name | ANDA |
| Labeler Name | Crown Laboratories |
| Substance Name | HYDROCORTISONE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
