NDC properties for NDC 9 24208-358
NDC item 24208035801
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-01 |
| NDC Item | 24208035801 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-01) / 1 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
NDC item 24208035805
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-05 |
| NDC Item | 24208035805 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |
NDC item 24208035810
| NDC 9 | 24208-358 |
|---|---|
| NDC 10 | 24208-358-10 |
| NDC Item | 24208035810 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-358-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 595435 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-12-14 |
| Marketing status | ACTIVE |
| NDA | NDA050804 |