Product NDC: | 60505-0171 |
Proprietary Name: | TRAMADOL HYDROCHLORIDE |
Non Proprietary Name: | TRAMADOL HYDROCHLORIDE |
Active Ingredient(s): | 50 mg/1 & nbsp; TRAMADOL HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60505-0171 |
Labeler Name: | Apotex Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075981 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020710 |
Package NDC: | 60505-0171-2 |
Package Description: | 500 TABLET, COATED in 1 BOTTLE (60505-0171-2) |
NDC Code | 60505-0171-2 |
Proprietary Name | TRAMADOL HYDROCHLORIDE |
Package Description | 500 TABLET, COATED in 1 BOTTLE (60505-0171-2) |
Product NDC | 60505-0171 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TRAMADOL HYDROCHLORIDE |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20020710 |
Marketing Category Name | ANDA |
Labeler Name | Apotex Corp. |
Substance Name | TRAMADOL HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |