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MILLIPRED
MILLIPRED - 16477-505-01 - (PREDNISOLONE)
Drug Information of MILLIPRED
| Product NDC: | 16477-505 |
| Proprietary Name: | MILLIPRED |
| Non Proprietary Name: | PREDNISOLONE |
| Active Ingredient(s): | 5 mg/5mg & nbsp; PREDNISOLONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MILLIPRED
| Product NDC: | 16477-505 |
| Labeler Name: | Laser Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080354 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081001 |
Package Information of MILLIPRED
| Package NDC: | 16477-505-01 |
| Package Description: | 5 mg in 1 BOTTLE (16477-505-01) |
NDC Information of MILLIPRED
| NDC Code | 16477-505-01 |
| Proprietary Name | MILLIPRED |
| Package Description | 5 mg in 1 BOTTLE (16477-505-01) |
| Product NDC | 16477-505 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PREDNISOLONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081001 |
| Marketing Category Name | ANDA |
| Labeler Name | Laser Pharmaceuticals, LLC |
| Substance Name | PREDNISOLONE |
| Strength Number | 5 |
| Strength Unit | mg/5mg |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
