NDC properties for NDC 9 24208-004
NDC item 24208000401
| NDC 9 | 24208-004 |
|---|---|
| NDC 10 | 24208-004-01 |
| NDC Item | 24208000401 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-004-01) / 2.5 mL in 1 BOTTLE, DROPPER |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-08-02 |
| Marketing status | ACTIVE |
| NDA | NDA021516 |
NDC item 24208000402
| NDC 9 | 24208-004 |
|---|---|
| NDC 10 | 24208-004-02 |
| NDC Item | 24208000402 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-004-02) / 2.5 mL in 1 BOTTLE, DROPPER |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-08-02 |
| Marketing status | ACTIVE |
| NDA | NDA021516 |
NDC item 24208000403
| NDC 9 | 24208-004 |
|---|---|
| NDC 10 | 24208-004-03 |
| NDC Item | 24208000403 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-004-03) / 5 mL in 1 BOTTLE, DROPPER |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2004-08-02 |
| Marketing status | ACTIVE |
| NDA | NDA021516 |