NDC properties for NDC 9 59676-312
NDC item 59676031200
| NDC 9 | 59676-312 |
|---|---|
| NDC 10 | 59676-312-00 |
| NDC Item | 59676031200 |
| packaging | 2 mL in 1 VIAL, MULTI-DOSE |
| BLA | BLA103234 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |
NDC item 59676031204
| NDC 9 | 59676-312 |
|---|---|
| NDC 10 | 59676-312-04 |
| NDC Item | 59676031204 |
| packaging | 4 VIAL, MULTI-DOSE in 1 CARTON (59676-312-04) / 2 mL in 1 VIAL, MULTI-DOSE (59676-312-00) |
| BLA | BLA103234 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |