NDC properties for NDC 9 51072-020
NDC item 51072002000
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-00 |
| NDC Item | 51072002000 |
| packaging | 900 mL in 1 BOTTLE (51072-020-00) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
NDC item 51072002001
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-01 |
| NDC Item | 51072002001 |
| packaging | 135 mL in 1 BOTTLE (51072-020-01) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
NDC item 51072002002
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-02 |
| NDC Item | 51072002002 |
| packaging | 560 mL in 1 BOTTLE (51072-020-02) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
NDC item 51072002003
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-03 |
| NDC Item | 51072002003 |
| packaging | 280 mL in 1 BOTTLE (51072-020-03) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |