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TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN - 57664-537-18 - (TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN)
Drug Information of TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
| Product NDC: | 57664-537 |
| 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: | 57664-537 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077184 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20051216 |
Package Information of TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
| Package NDC: | 57664-537-18 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (57664-537-18) |
NDC Information of TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
| NDC Code | 57664-537-18 |
| Proprietary Name | TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (57664-537-18) |
| Product NDC | 57664-537 |
| 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 | 20051216 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| 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] |
