NDC properties for NDC 9 59676-302
NDC item 59676030200
| NDC 9 | 59676-302 |
|---|---|
| NDC 10 | 59676-302-00 |
| NDC Item | 59676030200 |
| packaging | 1 mL in 1 VIAL, SINGLE-DOSE |
| BLA | BLA103234 |
| FDA SPL set id | 477378 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |
NDC item 59676030201
| NDC 9 | 59676-302 |
|---|---|
| NDC 10 | 59676-302-01 |
| NDC Item | 59676030201 |
| packaging | 6 VIAL, SINGLE-DOSE in 1 CARTON (59676-302-01) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-302-00) |
| BLA | BLA103234 |
| FDA SPL set id | 477378 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |