NDC properties for "eribulin mesylate 1 MG per 2 ML Injection" (RxCUI 1045456)
About this data
The tables show NDC propoerties for eribulin mesylate 1 MG per 2 ML Injection with the RxCUI 1045456
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for eribulin mesylate 1 MG per 2 ML Injection (RxCUI 1045456)
ANDA | ANDA214850 |
---|---|
ANDA | ANDA218047 |
ANDA | ANDA218281 |
MMSL_CODE | BD26641 |
MMSL_CODE | CD26641 |
RxCUI | 1045456 |
SPL_SET_ID | 4a64918a-f674-4843-b544-ab815fdd1b8f |
SPL_SET_ID | 7752b084-cdc7-6eac-e294-e45db82c372a |
SPL_SET_ID | aa69e7a5-fa82-4984-b9d2-653c772b80e3 |
SPL_SET_ID | f57835e2-4c53-4e93-b54b-7d7a5000ae3d |
VUID | 4030274 |
Prescribable Synonym | eriBULin mesylate 1 MG in 2 ML Injection |
RXNAV_STR | 2 ML eriBULin mesylate 0.5 MG/ML Injection |
RxNorm Name | 2 ML eribulin mesylate 0.5 MG/ML Injection |
RxNorm Synonym | eribulin mesylate 1 MG per 2 ML Injection |
Tallman Synonym | 2 ML eriBULin mesylate 0.5 MG/ML Injection |
Tallman Synonym | eriBULin mesylate 1 MG per 2 ML Injection |
Related queries | Interactions (for RxCUI 1045456) |
NDC Properties
NDC Item 00143916701
NDC 9 | 0143-9167 |
---|---|
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 |
Related queries | Properties for NDC 9 0143-9167 |
NDC Item 60505628900
NDC 9 | 60505-6289 |
---|---|
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 |
Related queries | Properties for NDC 9 60505-6289 |
NDC Item 68083059201
NDC 9 | 68083-592 |
---|---|
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 |
Related queries | Properties for NDC 9 68083-592 |
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 |
Related queries | Properties for NDC 9 81298-3890 |
NDC Item 00143916701
NDC 9 | 0143-9167 |
---|---|
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 |
Related queries | Properties for NDC 9 0143-9167 |
NDC Item 60505628900
NDC 9 | 60505-6289 |
---|---|
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 |
Related queries | Properties for NDC 9 60505-6289 |
NDC Item 68083059201
NDC 9 | 68083-592 |
---|---|
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 |
Related queries | Properties for NDC 9 68083-592 |
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 |
Related queries | Properties for NDC 9 81298-3890 |
NDC Item 00143916701
NDC 9 | 0143-9167 |
---|---|
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 |
Related queries | Properties for NDC 9 0143-9167 |
NDC Item 60505628900
NDC 9 | 60505-6289 |
---|---|
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 |
Related queries | Properties for NDC 9 60505-6289 |
NDC Item 68083059201
NDC 9 | 68083-592 |
---|---|
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 |
Related queries | Properties for NDC 9 68083-592 |
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 |
Related queries | Properties for NDC 9 81298-3890 |
NDC Item 00143916701
NDC 9 | 0143-9167 |
---|---|
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 |
Related queries | Properties for NDC 9 0143-9167 |
NDC Item 60505628900
NDC 9 | 60505-6289 |
---|---|
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 |
Related queries | Properties for NDC 9 60505-6289 |
NDC Item 68083059201
NDC 9 | 68083-592 |
---|---|
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 |
Related queries | Properties for NDC 9 68083-592 |
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 |
Related queries | Properties for NDC 9 81298-3890 |