NDC properties for NDC 9 0597-0545
NDC item 00597054522
NDC 9 | 0597-0545 |
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NDC 10 | 0597-0545-22 |
NDC Item | 00597054522 |
packaging | 2 KIT in 1 CARTON (0597-0545-22) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY (0597-0540-10) / .8 mL in 1 SYRINGE * 2 PACKET in 1 TRAY / 1 mL in 1 PACKET |
BLA | BLA761058 |
FDA SPL set id | 784593 |
Labeler | Boehringer Ingelheim Pharmaceuticals, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | BLA |
Marketing effective time low | 2023-10-01 |
Marketing status | ACTIVE |
NDC item 82009014822
NDC 9 | 82009-148 |
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NDC 10 | 82009-148-22 |
NDC Item | 82009014822 |
packaging | 2 KIT in 1 CARTON (82009-148-22) / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY (82009-149-11) / .8 mL in 1 SYRINGE * 2 PACKET in 1 TRAY / 1 mL in 1 PACKET |
BLA | BLA761058 |
FDA SPL set id | 784783 |
Labeler | QUALLENT PHARMACEUTICALS HEALTH LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | BLA |
Marketing effective time low | 2024-04-30 |
Marketing status | ACTIVE |
NDC item 82009014911
NDC 9 | 82009-149 |
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NDC 10 | 82009-149-11 |
NDC Item | 82009014911 |
packaging | 0.8 mL in 1 SYRINGE |
packaging | 1 in 1 TRAY |
FDA SPL set id | 784783 |
Labeler | QUALLENT PHARMACEUTICALS HEALTH LLC |
Label type | HUMAN PRESCRIPTION DRUG LABEL |