Product NDC: | 16477-510 |
Proprietary Name: | Millipred |
Non Proprietary Name: | PREDNISOLONE SODIUM PHOSPHATE |
Active Ingredient(s): | 10 mg/5mL & nbsp; PREDNISOLONE SODIUM PHOSPHATE |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16477-510 |
Labeler Name: | Laser Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078465 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090701 |
Package NDC: | 16477-510-08 |
Package Description: | 237 mL in 1 BOTTLE (16477-510-08) |
NDC Code | 16477-510-08 |
Proprietary Name | Millipred |
Package Description | 237 mL in 1 BOTTLE (16477-510-08) |
Product NDC | 16477-510 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PREDNISOLONE SODIUM PHOSPHATE |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20090701 |
Marketing Category Name | ANDA |
Labeler Name | Laser Pharmaceuticals, LLC |
Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
Strength Number | 10 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |