| NDC Code | 54868-3165-2 |
|---|
| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (54868-3165-2) |
|---|
| Product NDC | 54868-3165 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydromorphone Hydrochloride |
|---|
| Non-Proprietary Name | Hydromorphone Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20040920 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078273 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
|---|
| DEA Schedule | CII |
|---|