NDC properties for NDC 9 39822-0706
NDC item 39822070601
| NDC 9 | 39822-0706 |
|---|---|
| NDC 10 | 39822-0706-1 |
| NDC Item | 39822070601 |
| packaging | 1 in 1 VIAL |
| ANDA | ANDA064210 |
| Labeler | XGen Pharmaceuticals DJB, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1998-06-30 |
| Marketing status | ACTIVE |
NDC item 39822070602
| NDC 9 | 39822-0706 |
|---|---|
| NDC 10 | 39822-0706-2 |
| NDC Item | 39822070602 |
| packaging | 10 VIAL in 1 BOX (39822-0706-2) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0706-1) |
| ANDA | ANDA064210 |
| Labeler | XGen Pharmaceuticals DJB, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1998-06-30 |
| Marketing status | ACTIVE |