NDC properties for NDC 9 63323-305
NDC item 63323030501
NDC 9 | 63323-305 |
---|---|
NDC 10 | 63323-305-01 |
NDC Item | 63323030501 |
packaging | 2 mL in 1 VIAL, MULTI-DOSE |
ANDA | ANDA065122 |
FDA SPL set id | 773621 |
Labeler | Fresenius Kabi USA, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2004-11-30 |
Marketing status | ACTIVE |
NDC item 63323030502
NDC 9 | 63323-305 |
---|---|
NDC 10 | 63323-305-02 |
NDC Item | 63323030502 |
packaging | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-305-02) / 2 mL in 1 VIAL, MULTI-DOSE (63323-305-01) |
ANDA | ANDA065122 |
FDA SPL set id | 773621 |
Labeler | Fresenius Kabi USA, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2004-11-30 |
Marketing status | ACTIVE |
NDC item 68083025301
NDC 9 | 68083-253 |
---|---|
NDC 10 | 68083-253-01 |
NDC Item | 68083025301 |
packaging | 2 mL in 1 VIAL, MULTI-DOSE |
ANDA | ANDA209621 |
FDA SPL set id | 699468 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-02-11 |
Marketing status | ACTIVE |
NDC item 68083025325
NDC 9 | 68083-253 |
---|---|
NDC 10 | 68083-253-25 |
NDC Item | 68083025325 |
packaging | 25 VIAL, MULTI-DOSE in 1 CARTON (68083-253-25) / 2 mL in 1 VIAL, MULTI-DOSE (68083-253-01) |
ANDA | ANDA209621 |
FDA SPL set id | 699468 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-02-11 |
Marketing status | ACTIVE |