Home
>
National Drug Code (NDC)
>
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN - 68084-496-01 - (TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN)
Drug Information of TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
| Product NDC: | 68084-496 |
| Proprietary Name: | TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
| Non Proprietary Name: | TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
| Active Ingredient(s): | 325; 37.5 mg/1; mg/1 & nbsp; TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
| Product NDC: | 68084-496 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077184 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120301 |
Package Information of TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
| Package NDC: | 68084-496-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-496-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-496-11) |
NDC Information of TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
| NDC Code | 68084-496-01 |
| Proprietary Name | TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-496-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-496-11) |
| Product NDC | 68084-496 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
| Strength Number | 325; 37.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
