NDC properties for NDC 9 0065-0648
NDC item 00065064835
| NDC 9 | 0065-0648 |
|---|---|
| NDC 10 | 0065-0648-35 |
| NDC Item | 00065064835 |
| packaging | 1 TUBE in 1 CARTON (0065-0648-35) / 3.5 g in 1 TUBE |
| FDA SPL set id | 587764 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2022-06-30 |
| Marketing effective time low | 1988-10-15 |
| Marketing status | COMPLETED |
| NDA | NDA050616 |
NDC item 00078087601
| NDC 9 | 0078-0876 |
|---|---|
| NDC 10 | 0078-0876-01 |
| NDC Item | 00078087601 |
| packaging | 3.5 g in 1 TUBE (0078-0876-01) |
| FDA SPL set id | 861876 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-10-15 |
| Marketing status | ACTIVE |
| NDA | NDA050616 |
NDC item 00780087601
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 00780087601 |
NDC item 52959059203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959059203 |