NDC properties for NDC 9 54799-504
NDC item 54799050401
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-01 |
| NDC Item | 54799050401 |
| packaging | .6 mL in 1 BOTTLE, DROPPER (54799-504-01) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
NDC item 54799050405
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-05 |
| NDC Item | 54799050405 |
| packaging | 5 mL in 1 BOTTLE, DROPPER (54799-504-05) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
NDC item 54799050501
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-01 |
| NDC Item | 54799050501 |
| packaging | .6 mL in 1 BOTTLE, DROPPER (54799-505-01) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
NDC item 54799050505
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-05 |
| NDC Item | 54799050505 |
| packaging | 5 mL in 1 BOTTLE, DROPPER (54799-505-05) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |