NDC properties for NDC 9 69784-630
NDC item 69784063025
| NDC 9 | 69784-630 |
|---|---|
| NDC 10 | 69784-630-25 |
| NDC Item | 69784063025 |
| packaging | 1 BOTTLE in 1 CARTON (69784-630-25) / 25 TABLET in 1 BOTTLE |
| COLORTEXT | white(off-white) |
| Color | C48325 __ |
| FDA SPL set id | 682160 |
| Imprint code | T40 |
| Labeler | Woodward Pharma Services LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-06-30 |
| Marketing status | ACTIVE |
| NDA | NDA012429 |
| Score | 2 |
| Shape | C48348 |
| Size | 9 mm |
NDC item 76388088025
| NDC 9 | 76388-880 |
|---|---|
| NDC 10 | 76388-880-25 |
| NDC Item | 76388088025 |
| packaging | 1 BOTTLE in 1 CARTON (76388-880-25) / 25 TABLET in 1 BOTTLE |
| COLORTEXT | white(off-white) |
| Color | C48325 __ |
| FDA SPL set id | 650307 |
| Imprint code | T40 |
| Labeler | Aspen Global Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2025-03-31 |
| Marketing effective time low | 2013-03-12 |
| Marketing status | COMPLETED |
| NDA | NDA012429 |
| Score | 2 |
| Shape | C48348 |
| Size | 9 mm |
NDC item 80725063025
| NDC 9 | 80725-630 |
|---|---|
| NDC 10 | 80725-630-25 |
| NDC Item | 80725063025 |
| packaging | 1 BOTTLE in 1 CARTON (80725-630-25) / 25 TABLET in 1 BOTTLE |
| COLORTEXT | white(off-white) |
| Color | C48325 __ |
| FDA SPL set id | 710371 |
| Imprint code | T40 |
| Labeler | Waylis Therapeutics LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2023-05-15 |
| Marketing status | ACTIVE |
| NDA | NDA012429 |
| Score | 2 |
| Shape | C48348 |
| Size | 9 mm |