Prednisolone is a Oral Solution in the Human Prescription Drug category. It is labeled and distributed by Chartwell Rx, Llc. The primary component is Prednisolone.
Product ID | 62135-250_e8bb2605-e256-603d-e053-2995a90a5d7c |
NDC | 62135-250 |
Product Type | Human Prescription Drug |
Proprietary Name | Prednisolone |
Generic Name | Prednisolone Oral |
Dosage Form | Solution |
Route of Administration | ORAL |
Marketing Start Date | 1999-05-13 |
Marketing Category | ANDA / |
Application Number | ANDA040323 |
Labeler Name | Chartwell RX, LLC |
Substance Name | PREDNISOLONE |
Active Ingredient Strength | 15 mg/5mL |
Pharm Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2022-09-14 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
0527-5406 | PrednisoLONE | Prednisolone |
0603-1567 | PrednisoLONE | Prednisolone |
12634-686 | Prednisolone | Prednisolone |
21695-365 | Prednisolone | Prednisolone |
33261-475 | Prednisolone | Prednisolone |
50090-0655 | Prednisolone | Prednisolone |
50383-042 | Prednisolone | Prednisolone |
53217-193 | Prednisolone | Prednisolone |
58177-910 | Prednisolone | Prednisolone |
61919-291 | PREDNISOLONE | PREDNISOLONE |
62135-250 | Prednisolone | Prednisolone oral |
63187-466 | Prednisolone | Prednisolone |
63629-1862 | Prednisolone | Prednisolone |
66116-603 | Prednisolone | Prednisolone |
67296-1656 | Prednisolone | Prednisolone |
68258-8987 | Prednisolone | Prednisolone |
68788-7207 | PrednisoLONE | Prednisolone |
68788-9096 | Prednisolone | Prednisolone |
70518-2084 | Prednisolone | Prednisolone |
23594-505 | MILLIPRED | PREDNISOLONE |
73534-505 | MILLIPRED | PREDNISOLONE |
0378-4710 | Prednisolone Sodium Phosphate | prednisolone |
0378-4715 | Prednisolone Sodium Phosphate | prednisolone |
0378-4730 | Prednisolone Sodium Phosphate | prednisolone |