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Sufentanil Citrate
Sufentanil Citrate - 0409-3382-51 - (SUFENTANIL CITRATE)
Drug Information of Sufentanil Citrate
| Product NDC: | 0409-3382 |
| Proprietary Name: | Sufentanil Citrate |
| Non Proprietary Name: | SUFENTANIL CITRATE |
| Active Ingredient(s): | 50 ug/mL & nbsp; SUFENTANIL CITRATE |
| Administration Route(s): | EPIDURAL; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sufentanil Citrate
| Product NDC: | 0409-3382 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074534 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111011 |
Package Information of Sufentanil Citrate
| Package NDC: | 0409-3382-51 |
| Package Description: | 10 VIAL, SINGLE-USE in 1 CARTON (0409-3382-51) > 5 mL in 1 VIAL, SINGLE-USE |
NDC Information of Sufentanil Citrate
| NDC Code | 0409-3382-51 |
| Proprietary Name | Sufentanil Citrate |
| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (0409-3382-51) > 5 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0409-3382 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SUFENTANIL CITRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | EPIDURAL; INTRAVENOUS |
| Start Marketing Date | 20111011 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | SUFENTANIL CITRATE |
| Strength Number | 50 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
