| NDC Code | 72865-111-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (72865-111-05) |
|---|
| Product NDC | 72865-111 |
|---|
| 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 | 20200227 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211487 |
|---|
| Manufacturer | XLCare Pharmaceuticals, Inc. |
|---|
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
|---|
| Strength | 325; 7.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Opioid Agonist [EPC], Opioid Agonists [MoA] |
|---|
| DEA Schedule | CII |
|---|