Product NDC: | 49999-899 |
Proprietary Name: | Oxycodone Hydchloride |
Non Proprietary Name: | Oxycodone Hydchloride |
Active Ingredient(s): | 5 mg/1 & nbsp; Oxycodone Hydchloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49999-899 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091393 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111220 |
Package NDC: | 49999-899-00 |
Package Description: | 100 TABLET in 1 BOTTLE (49999-899-00) |
NDC Code | 49999-899-00 |
Proprietary Name | Oxycodone Hydchloride |
Package Description | 100 TABLET in 1 BOTTLE (49999-899-00) |
Product NDC | 49999-899 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Oxycodone Hydchloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20111220 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | OXYCODONE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |