NDC properties for NDC 9 70069-696
NDC item 70069069601
NDC 9 | 70069-696 |
---|---|
NDC 10 | 70069-696-01 |
NDC Item | 70069069601 |
packaging | 1 BOTTLE in 1 CARTON (70069-696-01) / 5 mL in 1 BOTTLE |
ANDA | ANDA216654 |
FDA SPL set id | 827154 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2024-10-31 |
Marketing status | ACTIVE |
NDC item 70069069701
NDC 9 | 70069-697 |
---|---|
NDC 10 | 70069-697-01 |
NDC Item | 70069069701 |
packaging | 1 BOTTLE in 1 CARTON (70069-697-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA216654 |
FDA SPL set id | 827154 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2024-10-31 |
Marketing status | ACTIVE |
NDC item 70069069801
NDC 9 | 70069-698 |
---|---|
NDC 10 | 70069-698-01 |
NDC Item | 70069069801 |
packaging | 1 BOTTLE in 1 CARTON (70069-698-01) / 15 mL in 1 BOTTLE |
ANDA | ANDA216654 |
FDA SPL set id | 827154 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2024-10-31 |
Marketing status | ACTIVE |