NDC properties for NDC 9 59676-312
NDC item 59676031200
NDC 9 | 59676-312 |
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NDC 10 | 59676-312-00 |
NDC Item | 59676031200 |
packaging | 2 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 59676031204
NDC 9 | 59676-312 |
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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 |
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 |