NDC properties for NDC 9 0023-9211
NDC item 00023921103
| NDC 9 | 0023-9211 |
|---|---|
| NDC 10 | 0023-9211-03 |
| NDC Item | 00023921103 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (0023-9211-03) / 2.5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 828126 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2007-11-14 |
| Marketing status | ACTIVE |
| NDA | NDA021398 |
NDC item 00023921105
| NDC 9 | 0023-9211 |
|---|---|
| NDC 10 | 0023-9211-05 |
| NDC Item | 00023921105 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (0023-9211-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 828126 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2007-11-14 |
| Marketing status | ACTIVE |
| NDA | NDA021398 |
NDC item 00023921110
| NDC 9 | 0023-9211 |
|---|---|
| NDC 10 | 0023-9211-10 |
| NDC Item | 00023921110 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (0023-9211-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 828126 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2007-11-14 |
| Marketing status | ACTIVE |
| NDA | NDA021398 |
NDC item 00023921115
| NDC 9 | 0023-9211 |
|---|---|
| NDC 10 | 0023-9211-15 |
| NDC Item | 00023921115 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (0023-9211-15) / 15 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 828126 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2007-11-14 |
| Marketing status | ACTIVE |
| NDA | NDA021398 |