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HYDROCORTISONE
HYDROCORTISONE - 16590-990-30 - (HYDROCORTISONE)
Drug Information of HYDROCORTISONE
| Product NDC: | 16590-990 |
| Proprietary Name: | HYDROCORTISONE |
| Non Proprietary Name: | HYDROCORTISONE |
| Active Ingredient(s): | 20 mg/1 & nbsp; HYDROCORTISONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HYDROCORTISONE
| Product NDC: | 16590-990 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083365 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19730618 |
Package Information of HYDROCORTISONE
| Package NDC: | 16590-990-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (16590-990-30) |
NDC Information of HYDROCORTISONE
| NDC Code | 16590-990-30 |
| Proprietary Name | HYDROCORTISONE |
| Package Description | 30 TABLET in 1 BOTTLE (16590-990-30) |
| Product NDC | 16590-990 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCORTISONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19730618 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | HYDROCORTISONE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
