NDC Code | 47335-037-40 |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (47335-037-40) > 5 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 47335-037 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydroxyprogesterone Caproate |
Non-Proprietary Name | Hydroxyprogesterone Caproate |
Dosage Form | INJECTION |
Usage | INTRAMUSCULAR |
Start Marketing Date | 20190701 |
Marketing Category Name | ANDA |
Application Number | ANDA208381 |
Manufacturer | Sun Pharmaceutical Industries, Inc. |
Substance Name | HYDROXYPROGESTERONE CAPROATE |
Strength | 250 |
Strength Unit | mg/mL |
Pharmacy Classes | Progesterone Congeners [CS], Progestin [EPC] |