NDC properties for NDC 9 59676-320
NDC item 59676032000
| NDC 9 | 59676-320 |
|---|---|
| NDC 10 | 59676-320-00 |
| NDC Item | 59676032000 |
| packaging | 1 mL in 1 VIAL, MULTI-DOSE |
| BLA | BLA103234 |
| FDA SPL set id | 785437 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |
NDC item 59676032004
| NDC 9 | 59676-320 |
|---|---|
| NDC 10 | 59676-320-04 |
| NDC Item | 59676032004 |
| packaging | 4 VIAL, MULTI-DOSE in 1 CARTON (59676-320-04) / 1 mL in 1 VIAL, MULTI-DOSE (59676-320-00) |
| BLA | BLA103234 |
| FDA SPL set id | 785437 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |