NDC Code | 60760-701-30 |
Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-701-30) |
Product NDC | 60760-701 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Morphine Sulfate |
Non-Proprietary Name | Morphine Sulfate |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20160401 |
Marketing Category Name | ANDA |
Application Number | ANDA203849 |
Manufacturer | St Marys Medical Park Pharmacy |
Substance Name | MORPHINE SULFATE |
Strength | 15 |
Strength Unit | mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |