Home
>
National Drug Code (NDC)
>
TRAMADOL HYDROCHLORIDE
TRAMADOL HYDROCHLORIDE - 47335-859-18 - (TRAMADOL HYDROCHLORIDE)
Drug Information of TRAMADOL HYDROCHLORIDE
| Product NDC: | 47335-859 |
| Proprietary Name: | TRAMADOL HYDROCHLORIDE |
| Non Proprietary Name: | TRAMADOL HYDROCHLORIDE |
| Active Ingredient(s): | 100 mg/1 & nbsp; TRAMADOL HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRAMADOL HYDROCHLORIDE
| Product NDC: | 47335-859 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201384 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111212 |
Package Information of TRAMADOL HYDROCHLORIDE
| Package NDC: | 47335-859-18 |
| Package Description: | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-18) |
NDC Information of TRAMADOL HYDROCHLORIDE
| NDC Code | 47335-859-18 |
| Proprietary Name | TRAMADOL HYDROCHLORIDE |
| Package Description | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-18) |
| Product NDC | 47335-859 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRAMADOL HYDROCHLORIDE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20111212 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
