NDC properties for NDC 9 0143-9167
NDC item 00143916701
NDC 9 | 0143-9167 |
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NDC 10 | 0143-9167-01 |
NDC Item | 00143916701 |
packaging | 1 VIAL, SINGLE-DOSE in 1 CARTON (0143-9167-01) / 2 mL in 1 VIAL, SINGLE-DOSE |
ANDA | ANDA218281 |
FDA SPL set id | 796857 |
Labeler | HIKMA PHARMACEUTICALS USA INC. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2024-06-28 |
Marketing status | active |
NDC item 60505628900
NDC 9 | 60505-6289 |
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NDC 10 | 60505-6289-0 |
NDC Item | 60505628900 |
packaging | 1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6289-0) / 2 mL in 1 VIAL, SINGLE-DOSE |
ANDA | ANDA218047 |
FDA SPL set id | 785024 |
Labeler | Apotex Corp. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2024-05-06 |
Marketing status | ACTIVE |
NDC item 68083059201
NDC 9 | 68083-592 |
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NDC 10 | 68083-592-01 |
NDC Item | 68083059201 |
packaging | 1 VIAL, SINGLE-DOSE in 1 CARTON (68083-592-01) / 2 mL in 1 VIAL, SINGLE-DOSE |
ANDA | ANDA218047 |
FDA SPL set id | 780904 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2024-04-05 |
Marketing status | ACTIVE |
NDC item 81298389001
NDC 9 | 81298-3890 |
---|---|
NDC 10 | 81298-3890-1 |
NDC Item | 81298389001 |
packaging | 1 VIAL, SINGLE-DOSE in 1 CARTON (81298-3890-1) / 2 mL in 1 VIAL, SINGLE-DOSE |
ANDA | ANDA214850 |
FDA SPL set id | 800808 |
Labeler | Long Grove Pharmaceuticals, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2024-07-22 |
Marketing status | active |