| NDC Code | 0785-1122-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0785-1122-01) |
|---|
| Product NDC | 0785-1122 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lorcet Plus |
|---|
| Non-Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19841231 |
|---|
| End Marketing Date | 20140627 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA089689 |
|---|
| Manufacturer | Forest Laboratories, Inc. |
|---|
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
|---|
| Strength | 650; 7.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
|---|
| DEA Schedule | CIII |
|---|