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TRAMADOL HYDROCHLORIDE
TRAMADOL HYDROCHLORIDE - 49884-822-05 - (tramadol hydrochloride)
Drug Information of TRAMADOL HYDROCHLORIDE
| Product NDC: | 49884-822 |
| Proprietary Name: | TRAMADOL HYDROCHLORIDE |
| Non Proprietary Name: | tramadol hydrochloride |
| Active Ingredient(s): | 200 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: | 49884-822 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078783 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091113 |
Package Information of TRAMADOL HYDROCHLORIDE
| Package NDC: | 49884-822-05 |
| Package Description: | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-822-05) |
NDC Information of TRAMADOL HYDROCHLORIDE
| NDC Code | 49884-822-05 |
| Proprietary Name | TRAMADOL HYDROCHLORIDE |
| Package Description | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-822-05) |
| Product NDC | 49884-822 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tramadol hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20091113 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
