NDC properties for NDC 9 10122-820
NDC item 10122082004
| NDC 9 | 10122-820 |
|---|---|
| NDC 10 | 10122-820-04 |
| NDC Item | 10122082004 |
| packaging | 4 AMPULE in 1 POUCH (10122-820-04) / 4 mL in 1 AMPULE |
| FDA SPL set id | 696600 |
| Labeler | Chiesi USA, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2013-04-15 |
| Marketing status | ACTIVE |
| NDA | NDA201820 |
NDC item 10122082028
| NDC 9 | 10122-820 |
|---|---|
| NDC 10 | 10122-820-28 |
| NDC Item | 10122082028 |
| packaging | 7 POUCH in 1 CARTON (10122-820-28) / 4 AMPULE in 1 POUCH / 4 mL in 1 AMPULE |
| FDA SPL set id | 696600 |
| Labeler | Chiesi USA, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2013-04-15 |
| Marketing status | ACTIVE |
| NDA | NDA201820 |
NDC item 10122082056
| NDC 9 | 10122-820 |
|---|---|
| NDC 10 | 10122-820-56 |
| NDC Item | 10122082056 |
| packaging | 14 POUCH in 1 CARTON (10122-820-56) / 4 AMPULE in 1 POUCH / 4 mL in 1 AMPULE |
| FDA SPL set id | 696600 |
| Labeler | Chiesi USA, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2013-04-15 |
| Marketing status | ACTIVE |
| NDA | NDA201820 |