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HYDROCORTISONE
HYDROCORTISONE - 54505-333-10 - (hydrocortisone)
Drug Information of HYDROCORTISONE
| Product NDC: | 54505-333 |
| 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: | 54505-333 |
| Labeler Name: | Lineage Therapeutics Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040646 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070330 |
Package Information of HYDROCORTISONE
| Package NDC: | 54505-333-10 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (54505-333-10) |
NDC Information of HYDROCORTISONE
| NDC Code | 54505-333-10 |
| Proprietary Name | HYDROCORTISONE |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (54505-333-10) |
| Product NDC | 54505-333 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070330 |
| Marketing Category Name | ANDA |
| Labeler Name | Lineage Therapeutics Inc |
| Substance Name | HYDROCORTISONE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
