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Ala Scalp
Ala Scalp - 0316-0140-03 - (Hydrocortisone Acetate)
Drug Information of Ala Scalp
| Product NDC: | 0316-0140 |
| Proprietary Name: | Ala Scalp |
| Non Proprietary Name: | Hydrocortisone Acetate |
| Active Ingredient(s): | 20 mg/mL & nbsp; Hydrocortisone Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ala Scalp
| Product NDC: | 0316-0140 |
| Labeler Name: | Crown Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083231 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19730228 |
Package Information of Ala Scalp
| Package NDC: | 0316-0140-03 |
| Package Description: | 3 mL in 1 POUCH (0316-0140-03) |
NDC Information of Ala Scalp
| NDC Code | 0316-0140-03 |
| Proprietary Name | Ala Scalp |
| Package Description | 3 mL in 1 POUCH (0316-0140-03) |
| Product NDC | 0316-0140 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Acetate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19730228 |
| Marketing Category Name | ANDA |
| Labeler Name | Crown Laboratories |
| Substance Name | HYDROCORTISONE ACETATE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
