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Prednisolone
Prednisolone - 21695-365-08 - (Prednisolone)
Drug Information of Prednisolone
| Product NDC: | 21695-365 |
| Proprietary Name: | Prednisolone |
| Non Proprietary Name: | Prednisolone |
| Active Ingredient(s): | 15 mg/5mL & nbsp; Prednisolone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prednisolone
| Product NDC: | 21695-365 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040401 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030227 |
Package Information of Prednisolone
| Package NDC: | 21695-365-08 |
| Package Description: | 240 mL in 1 BOTTLE (21695-365-08) |
NDC Information of Prednisolone
| NDC Code | 21695-365-08 |
| Proprietary Name | Prednisolone |
| Package Description | 240 mL in 1 BOTTLE (21695-365-08) |
| Product NDC | 21695-365 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Prednisolone |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20030227 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | PREDNISOLONE |
| Strength Number | 15 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
