NDC properties for NDC 9 0703-4636
NDC item 00703463601
| NDC 9 | 0703-4636 |
|---|---|
| NDC 10 | 0703-4636-01 |
| NDC Item | 00703463601 |
| packaging | 10 mL in 1 VIAL (0703-4636-01) |
| Labeler | Teva Parenteral Medicines, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2003-12-03 |
| Marketing status | COMPLETED |
| NDA | NDA050577 |
NDC item 26060953004
| NDC 9 | 26060-9530 |
|---|---|
| NDC 10 | 26060-9530-4 |
| NDC Item | 26060953004 |
NDC item 68118010001
| NDC 9 | 68118-100 |
|---|---|
| NDC 10 | 68118-100-01 |
| NDC Item | 68118010001 |
| packaging | 1 VIAL, GLASS in 1 CARTON (68118-100-01) / 10 mL in 1 VIAL, GLASS |
| Labeler | ESTEVE PHARMACEUTICALS, S.A. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Marketing effective time low | 2025-05-19 |
| Marketing status | ACTIVE |
| UNAPPROVED_DRUG_FOR_USE_IN_DRUG_SHORTAGE | N/A |