NDC properties for NDC 9 0069-1307
NDC item 00069130701
| NDC 9 | 0069-1307 |
|---|---|
| NDC 10 | 0069-1307-01 |
| NDC Item | 00069130701 |
| packaging | 1 mL in 1 VIAL, SINGLE-DOSE |
| BLA | BLA125545 |
| Labeler | Pfizer Laboratories Div Pfizer Inc |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2018-06-18 |
| Marketing status | ACTIVE |
NDC item 00069130710
| NDC 9 | 0069-1307 |
|---|---|
| NDC 10 | 0069-1307-10 |
| NDC Item | 00069130710 |
| packaging | 10 VIAL, SINGLE-DOSE in 1 CARTON (0069-1307-10) / 1 mL in 1 VIAL, SINGLE-DOSE (0069-1307-01) |
| BLA | BLA125545 |
| Labeler | Pfizer Laboratories Div Pfizer Inc |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2018-06-18 |
| Marketing status | ACTIVE |
NDC item 59353000401
| NDC 9 | 59353-004 |
|---|---|
| NDC 10 | 59353-004-01 |
| NDC Item | 59353000401 |
| packaging | 1 mL in 1 VIAL, SINGLE-DOSE |
| BLA | BLA125545 |
| Labeler | Vifor (International) Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2018-06-18 |
| Marketing status | ACTIVE |
NDC item 59353000410
| NDC 9 | 59353-004 |
|---|---|
| NDC 10 | 59353-004-10 |
| NDC Item | 59353000410 |
| packaging | 10 VIAL, SINGLE-DOSE in 1 CARTON (59353-004-10) / 1 mL in 1 VIAL, SINGLE-DOSE (59353-004-01) |
| BLA | BLA125545 |
| Labeler | Vifor (International) Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 2018-06-18 |
| Marketing status | ACTIVE |