NDC properties for "Procrit" (RxCUI 205913)
About this data
The tables show NDC propoerties for Procrit with the RxCUI 205913
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 205913)
| BLA | BLA103234 |
|---|---|
| MMSL_CODE | BD1401 |
| RxCUI | 205913 |
| SPL_SET_ID | 0c721ba4-ae19-417f-aae1-221ed1a0866a |
| Prescribable Synonym | PROCRIT 10,000 UNT/ML Injectable Solution |
| RXNAV_STR | Procrit 10,000 UNT/ML Injectable Solution |
| RxNorm Name | epoetin alfa 10000 UNT/ML Injectable Solution [Procrit] |
| RxNorm Synonym | EPO 10000 UNT/ML Injectable Solution [Procrit] |
| RxNorm Synonym | ERYTHROPOIETIN 10000 UNT/ML Injectable Solution [Procrit] |
| RxNorm Synonym | Procrit 10,000 UNT/ML Injectable Solution |
| Related queries | Interactions (for RxCUI 205913) |
NDC Properties
NDC Item 59676031200
| NDC 9 | 59676-312 |
|---|---|
| NDC 10 | 59676-312-00 |
| NDC Item | 59676031200 |
| Packaging | 2 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 59676-312 |
NDC Item 59676031204
| NDC 9 | 59676-312 |
|---|---|
| NDC 10 | 59676-312-04 |
| NDC Item | 59676031204 |
| Packaging | 4 VIAL, MULTI-DOSE in 1 CARTON (59676-312-04) / 2 mL in 1 VIAL, MULTI-DOSE (59676-312-00) |
| 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 59676-312 |
NDC Item 59676031200
| NDC 9 | 59676-312 |
|---|---|
| NDC 10 | 59676-312-00 |
| NDC Item | 59676031200 |
| Packaging | 2 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 59676-312 |
NDC Item 59676031204
| NDC 9 | 59676-312 |
|---|---|
| NDC 10 | 59676-312-04 |
| NDC Item | 59676031204 |
| Packaging | 4 VIAL, MULTI-DOSE in 1 CARTON (59676-312-04) / 2 mL in 1 VIAL, MULTI-DOSE (59676-312-00) |
| 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 59676-312 |