NDC properties for NDC 9 50742-287
NDC item 50742028704
NDC 9 | 50742-287 |
---|---|
NDC 10 | 50742-287-04 |
NDC Item | 50742028704 |
packaging | 0.3 mL in 1 CONTAINER |
packaging | 4 in 1 POUCH |
ANDA | ANDA216533 |
FDA SPL set id | 749629 |
Labeler | Ingenus Pharmaceuticals, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-15 |
Marketing status | ACTIVE |
NDC item 50742028760
NDC 9 | 50742-287 |
---|---|
NDC 10 | 50742-287-60 |
NDC Item | 50742028760 |
packaging | 15 POUCH in 1 CARTON (50742-287-60) / 4 CONTAINER in 1 POUCH (50742-287-04) / .3 mL in 1 CONTAINER |
ANDA | ANDA216533 |
FDA SPL set id | 749629 |
Labeler | Ingenus Pharmaceuticals, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-15 |
Marketing status | ACTIVE |