NDC Code | 54868-4598-3 |
Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (54868-4598-3) |
Product NDC | 54868-4598 |
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 | 20020206 |
Marketing Category Name | ANDA |
Application Number | ANDA076855 |
Manufacturer | Physicians Total Care, Inc. |
Substance Name | HYDROMORPHONE HYDROCHLORIDE |
Strength | 8 |
Strength Unit | mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |