| NDC Code | 68084-368-01 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-368-01) > 10 TABLET in 1 BLISTER PACK (68084-368-11) |
|---|
| Product NDC | 68084-368 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
|---|
| Non-Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090922 |
|---|
| End Marketing Date | 20161006 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040736 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | HYDROCODONE BITARTRATE; ACETAMINOPHEN |
|---|
| Strength | 5; 325 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
|---|
| DEA Schedule | CIII |
|---|