NDC Code | 42858-302-25 |
Package Description | 4 BLISTER PACK in 1 CARTON (42858-302-25) / 25 TABLET in 1 BLISTER PACK |
Product NDC | 42858-302 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydromorphone Hydrochloride |
Non-Proprietary Name | Hydromorphone Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20091123 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA019892 |
Manufacturer | Rhodes Pharmaceuticals L.P. |
Substance Name | HYDROMORPHONE HYDROCHLORIDE |
Strength | 4 |
Strength Unit | mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
DEA Schedule | CII |