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Hydrocortisone Acetate
Hydrocortisone Acetate - 0574-7090-12 - (HYDROCORTISONE ACETATE)
Drug Information of Hydrocortisone Acetate
| Product NDC: | 0574-7090 |
| Proprietary Name: | Hydrocortisone Acetate |
| Non Proprietary Name: | HYDROCORTISONE ACETATE |
| Active Ingredient(s): | 25 mg/1 & nbsp; HYDROCORTISONE ACETATE |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone Acetate
| Product NDC: | 0574-7090 |
| Labeler Name: | Paddock Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900701 |
Package Information of Hydrocortisone Acetate
| Package NDC: | 0574-7090-12 |
| Package Description: | 12 PACKET in 1 BOX (0574-7090-12) > 1 SUPPOSITORY in 1 PACKET |
NDC Information of Hydrocortisone Acetate
| NDC Code | 0574-7090-12 |
| Proprietary Name | Hydrocortisone Acetate |
| Package Description | 12 PACKET in 1 BOX (0574-7090-12) > 1 SUPPOSITORY in 1 PACKET |
| Product NDC | 0574-7090 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCORTISONE ACETATE |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19900701 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Paddock Laboratories, LLC |
| Substance Name | HYDROCORTISONE ACETATE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
