NDC properties for NDC 9 59676-310
NDC item 59676031000
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-00 |
| NDC Item | 59676031000 |
| packaging | 1 mL in 1 VIAL, SINGLE-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 59676031001
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-01 |
| NDC Item | 59676031001 |
| packaging | 6 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-01) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00) |
| 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 |
NDC item 59676031002
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-02 |
| NDC Item | 59676031002 |
| packaging | 25 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-02) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00) |
| 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 |