| NDC Code | 33342-202-15 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (33342-202-15) |
|---|
| Product NDC | 33342-202 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Tramadol Hydrochloride And Acetaminophen |
|---|
| Non-Proprietary Name | Tramadol Hydrochloride And Acetaminophen |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170503 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA206885 |
|---|
| Manufacturer | Macleods Pharmaceuticals Limited |
|---|
| Substance Name | TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN |
|---|
| Strength | 37.5; 325 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
|---|
| DEA Schedule | CIV |
|---|