NDC properties for NDC 9 51759-412
NDC item 51759041222
NDC 9 | 51759-412 |
---|---|
NDC 10 | 51759-412-22 |
NDC Item | 51759041222 |
packaging | 2 KIT in 1 CARTON (51759-412-22) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .4 mL in 1 SYRINGE (51759-624-31) * .4 mL in 1 POUCH |
BLA | BLA761299 |
FDA SPL set id | 800492 |
Labeler | Teva Pharmaceuticals USA, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | BLA |
Marketing effective time low | 2024-07-31 |
Marketing status | active |
NDC item 51759062431
NDC 9 | 51759-624 |
---|---|
NDC 10 | 51759-624-31 |
NDC Item | 51759062431 |
packaging | 0.4 mL in 1 SYRINGE |
FDA SPL set id | 800492 |
Labeler | Teva Pharmaceuticals USA, Inc. |
Label type | HUMAN PRESCRIPTION DRUG LABEL |