NDC properties for "Procrit" (RxCUI 205918)
About this data
The tables show NDC propoerties for Procrit with the RxCUI 205918
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 205918)
| BLA | BLA103234 |
|---|---|
| MMSL_CODE | BD1403 |
| MMSL_CODE | BD30445 |
| RxCUI | 205918 |
| SPL_SET_ID | 0c721ba4-ae19-417f-aae1-221ed1a0866a |
| Prescribable Synonym | PROCRIT 2000 UNT in 1 ML Injection |
| RXNAV_STR | 1 ML Procrit 2000 UNT/ML Injection |
| RxNorm Name | 1 ML epoetin alfa 2000 UNT/ML Injection [Procrit] |
| RxNorm Synonym | 1 ML EPO 2000 UNT/ML Injection [Procrit] |
| RxNorm Synonym | 1 ML ERYTHROPOIETIN 2000 UNT/ML Injection [Procrit] |
| RxNorm Synonym | 1 ML Procrit 2000 UNT/ML Injection |
| RxNorm Synonym | Procrit 2000 UNT per 1 ML Injection |
| Related queries | Interactions (for RxCUI 205918) |
NDC Properties
NDC Item 59676030200
| NDC 9 | 59676-302 |
|---|---|
| NDC 10 | 59676-302-00 |
| NDC Item | 59676030200 |
| Packaging | 1 mL in 1 VIAL, SINGLE-DOSE |
| BLA | BLA103234 |
| FDA SPL set id | 477378 |
| 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 59676-302 |
NDC Item 59676030201
| NDC 9 | 59676-302 |
|---|---|
| NDC 10 | 59676-302-01 |
| NDC Item | 59676030201 |
| Packaging | 6 VIAL, SINGLE-DOSE in 1 CARTON (59676-302-01) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-302-00) |
| BLA | BLA103234 |
| FDA SPL set id | 477378 |
| 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 59676-302 |
NDC Item 59676030200
| NDC 9 | 59676-302 |
|---|---|
| NDC 10 | 59676-302-00 |
| NDC Item | 59676030200 |
| Packaging | 1 mL in 1 VIAL, SINGLE-DOSE |
| BLA | BLA103234 |
| FDA SPL set id | 477378 |
| 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 59676-302 |
NDC Item 59676030201
| NDC 9 | 59676-302 |
|---|---|
| NDC 10 | 59676-302-01 |
| NDC Item | 59676030201 |
| Packaging | 6 VIAL, SINGLE-DOSE in 1 CARTON (59676-302-01) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-302-00) |
| BLA | BLA103234 |
| FDA SPL set id | 477378 |
| 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 59676-302 |