NDC properties for NDC 9 69420-3077
NDC item 69420307701
NDC 9 | 69420-3077 |
---|---|
NDC 10 | 69420-3077-1 |
NDC Item | 69420307701 |
packaging | 30 g in 1 TUBE, WITH APPLICATOR (69420-3077-1) |
FDA SPL set id | 510238 |
Labeler | SA3, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA AUTHORIZED GENERIC |
Marketing effective time low | 2020-03-13 |
Marketing status | COMPLETED |
NDA_AUTHORIZED_GENERIC | NDA021717 |
NDC item 71800063104
NDC 9 | 71800-631 |
---|---|
NDC 10 | 71800-631-04 |
NDC Item | 71800063104 |
packaging | 4 TUBE in 1 CARTON (71800-631-04) / 30 g in 1 TUBE |
FDA SPL set id | 591823 |
Labeler | Innovida Pharmaceutique Corporation |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA AUTHORIZED GENERIC |
Marketing effective time low | 2017-05-03 |
Marketing status | COMPLETED |
NDA_AUTHORIZED_GENERIC | NDA021717 |
NDC item 71800063108
NDC 9 | 71800-631 |
---|---|
NDC 10 | 71800-631-08 |
NDC Item | 71800063108 |
packaging | 8 TUBE in 1 CARTON (71800-631-08) / 30 g in 1 TUBE |
FDA SPL set id | 591823 |
Labeler | Innovida Pharmaceutique Corporation |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA AUTHORIZED GENERIC |
Marketing effective time low | 2017-05-03 |
Marketing status | COMPLETED |
NDA_AUTHORIZED_GENERIC | NDA021717 |
NDC item 71800063115
NDC 9 | 71800-631 |
---|---|
NDC 10 | 71800-631-15 |
NDC Item | 71800063115 |
packaging | 1 TUBE in 1 CARTON (71800-631-15) / 30 g in 1 TUBE |
FDA SPL set id | 591823 |
Labeler | Innovida Pharmaceutique Corporation |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA AUTHORIZED GENERIC |
Marketing effective time low | 2017-05-03 |
Marketing status | COMPLETED |
NDA_AUTHORIZED_GENERIC | NDA021717 |