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Proctocream
Proctocream - 68220-141-30 - (Hydrocortisone)
Drug Information of Proctocream
| Product NDC: | 68220-141 |
| Proprietary Name: | Proctocream |
| 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 Proctocream
| Product NDC: | 68220-141 |
| Labeler Name: | Alaven Pharmaceutical LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089414 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110318 |
Package Information of Proctocream
| Package NDC: | 68220-141-30 |
| Package Description: | 1 TUBE in 1 CARTON (68220-141-30) > 30 g in 1 TUBE |
NDC Information of Proctocream
| NDC Code | 68220-141-30 |
| Proprietary Name | Proctocream |
| Package Description | 1 TUBE in 1 CARTON (68220-141-30) > 30 g in 1 TUBE |
| Product NDC | 68220-141 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110318 |
| Marketing Category Name | ANDA |
| Labeler Name | Alaven Pharmaceutical LLC |
| Substance Name | HYDROCORTISONE |
| Strength Number | 25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
