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Sufentanil Citrate
Sufentanil Citrate - 0641-6111-10 - (Sufentanil Citrate)
Drug Information of Sufentanil Citrate
| Product NDC: | 0641-6111 |
| Proprietary Name: | Sufentanil Citrate |
| Non Proprietary Name: | Sufentanil Citrate |
| Active Ingredient(s): | .05 mg/mL & nbsp; Sufentanil Citrate |
| Administration Route(s): | EPIDURAL; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sufentanil Citrate
| Product NDC: | 0641-6111 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074413 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19951215 |
Package Information of Sufentanil Citrate
| Package NDC: | 0641-6111-10 |
| Package Description: | 10 AMPULE in 1 CARTON (0641-6111-10) > 2 mL in 1 AMPULE (0641-6111-01) |
NDC Information of Sufentanil Citrate
| NDC Code | 0641-6111-10 |
| Proprietary Name | Sufentanil Citrate |
| Package Description | 10 AMPULE in 1 CARTON (0641-6111-10) > 2 mL in 1 AMPULE (0641-6111-01) |
| Product NDC | 0641-6111 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sufentanil Citrate |
| Dosage Form Name | INJECTION |
| Route Name | EPIDURAL; INTRAVENOUS |
| Start Marketing Date | 19951215 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | SUFENTANIL CITRATE |
| Strength Number | .05 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
