NDC properties for "Procrit" (RxCUI 1721690)
About this data
The tables show NDC propoerties for Procrit with the RxCUI 1721690
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 1721690)
| BLA | BLA103234 |
|---|---|
| MMSL_CODE | BD30444 |
| RxCUI | 1721690 |
| SPL_SET_ID | 0c721ba4-ae19-417f-aae1-221ed1a0866a |
| SPL_SET_ID | 9bbe9a5b-ad1d-41a4-9699-ff6dc776bce1 |
| Prescribable Synonym | PROCRIT 10,000 UNT in 1 ML Injection |
| RXNAV_STR | 1 ML Procrit 10000 UNT/ML Injection |
| RxNorm Name | 1 ML epoetin alfa 10000 UNT/ML Injection [Procrit] |
| RxNorm Synonym | 1 ML EPO 10000 UNT/ML Injection [Procrit] |
| RxNorm Synonym | 1 ML ERYTHROPOIETIN 10000 UNT/ML Injection [Procrit] |
| RxNorm Synonym | 1 ML Procrit 10000 UNT/ML Injection |
| RxNorm Synonym | Procrit 10,000 UNT per 1 ML Injection |
| Related queries | Interactions (for RxCUI 1721690) |
NDC Properties
NDC Item 59676031000
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-00 |
| NDC Item | 59676031000 |
| Packaging | 1 mL in 1 VIAL, SINGLE-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 59676-310 |
NDC Item 59676031001
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-01 |
| NDC Item | 59676031001 |
| Packaging | 6 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-01) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00) |
| 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 59676-310 |
NDC Item 59676031002
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-02 |
| NDC Item | 59676031002 |
| Packaging | 25 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-02) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00) |
| 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 59676-310 |
NDC Item 59676031000
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-00 |
| NDC Item | 59676031000 |
| Packaging | 1 mL in 1 VIAL, SINGLE-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 59676-310 |
NDC Item 59676031001
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-01 |
| NDC Item | 59676031001 |
| Packaging | 6 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-01) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00) |
| 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 59676-310 |
NDC Item 59676031002
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-02 |
| NDC Item | 59676031002 |
| Packaging | 25 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-02) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00) |
| 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 59676-310 |
NDC Item 59676031000
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-00 |
| NDC Item | 59676031000 |
| Packaging | 1 mL in 1 VIAL, SINGLE-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 59676-310 |
NDC Item 59676031001
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-01 |
| NDC Item | 59676031001 |
| Packaging | 6 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-01) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00) |
| 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 59676-310 |
NDC Item 59676031002
| NDC 9 | 59676-310 |
|---|---|
| NDC 10 | 59676-310-02 |
| NDC Item | 59676031002 |
| Packaging | 25 VIAL, SINGLE-DOSE in 1 CARTON (59676-310-02) / 1 mL in 1 VIAL, SINGLE-DOSE (59676-310-00) |
| 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 59676-310 |