NDC properties for "Procrit" (RxCUI 212219)
About this data
The tables show NDC propoerties for Procrit with the RxCUI 212219
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 Procrit (RxCUI 212219)
| BLA | BLA103234 |
|---|---|
| MMSL_CODE | BD5690 |
| RxCUI | 212219 |
| SPL_SET_ID | 0c721ba4-ae19-417f-aae1-221ed1a0866a |
| SPL_SET_ID | 9bbe9a5b-ad1d-41a4-9699-ff6dc776bce1 |
| Prescribable Synonym | PROCRIT 20,000 UNT/ML Injectable Solution |
| RXNAV_STR | Procrit 20000 UNT/ML Injectable Solution |
| RxNorm Name | epoetin alfa 20000 UNT/ML Injectable Solution [Procrit] |
| RxNorm Synonym | EPO 20000 UNT/ML Injectable Solution [Procrit] |
| RxNorm Synonym | ERYTHROPOIETIN 20000 UNT/ML Injectable Solution [Procrit] |
| RxNorm Synonym | Procrit 20000 UNT/ML Injectable Solution |
| Related queries | Interactions (for RxCUI 212219) |
NDC Properties
NDC Item 59676032000
| NDC 9 | 59676-320 |
|---|---|
| NDC 10 | 59676-320-00 |
| NDC Item | 59676032000 |
| Packaging | 1 mL in 1 VIAL, MULTI-DOSE |
| BLA | BLA103234 |
| FDA SPL set id | 785437 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 59676-320 |
NDC Item 59676032004
| NDC 9 | 59676-320 |
|---|---|
| NDC 10 | 59676-320-04 |
| NDC Item | 59676032004 |
| Packaging | 4 VIAL, MULTI-DOSE in 1 CARTON (59676-320-04) / 1 mL in 1 VIAL, MULTI-DOSE (59676-320-00) |
| BLA | BLA103234 |
| FDA SPL set id | 785437 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 59676-320 |
NDC Item 59676032000
| NDC 9 | 59676-320 |
|---|---|
| NDC 10 | 59676-320-00 |
| NDC Item | 59676032000 |
| Packaging | 1 mL in 1 VIAL, MULTI-DOSE |
| BLA | BLA103234 |
| FDA SPL set id | 785437 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 59676-320 |
NDC Item 59676032004
| NDC 9 | 59676-320 |
|---|---|
| NDC 10 | 59676-320-04 |
| NDC Item | 59676032004 |
| Packaging | 4 VIAL, MULTI-DOSE in 1 CARTON (59676-320-04) / 1 mL in 1 VIAL, MULTI-DOSE (59676-320-00) |
| BLA | BLA103234 |
| FDA SPL set id | 785437 |
| Labeler | Janssen Products, LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Marketing effective time low | 1989-06-01 |
| Marketing status | ACTIVE |
| Related queries | Properties for NDC 9 59676-320 |