NDC properties for NDC 9 60505-6124
NDC item 60505612400
| NDC 9 | 60505-6124 |
|---|---|
| NDC 10 | 60505-6124-0 |
| NDC Item | 60505612400 |
| packaging | 20 mL in 1 VIAL, SINGLE-DOSE |
| ANDA | ANDA208075 |
| Labeler | Apotex Corp. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2026-02-12 |
| Marketing status | ACTIVE |
NDC item 60505612401
| NDC 9 | 60505-6124 |
|---|---|
| NDC 10 | 60505-6124-1 |
| NDC Item | 60505612401 |
| packaging | 10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6124-1) / 20 mL in 1 VIAL, SINGLE-DOSE (60505-6124-0) |
| ANDA | ANDA208075 |
| Labeler | Apotex Corp. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2026-02-12 |
| Marketing status | ACTIVE |