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ANUCORT-HC
ANUCORT-HC - 0713-0503-01 - (Hydrocortisone Acetate)
Drug Information of ANUCORT-HC
| Product NDC: | 0713-0503 |
| Proprietary Name: | ANUCORT-HC |
| 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 ANUCORT-HC
| Product NDC: | 0713-0503 |
| Labeler Name: | G&W Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900115 |
Package Information of ANUCORT-HC
| Package NDC: | 0713-0503-01 |
| Package Description: | 100 SUPPOSITORY in 1 CARTON (0713-0503-01) |
NDC Information of ANUCORT-HC
| NDC Code | 0713-0503-01 |
| Proprietary Name | ANUCORT-HC |
| Package Description | 100 SUPPOSITORY in 1 CARTON (0713-0503-01) |
| Product NDC | 0713-0503 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Acetate |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19900115 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | G&W Laboratories, Inc. |
| Substance Name | HYDROCORTISONE ACETATE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
