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Alfentanil Hydrochloride
Alfentanil Hydrochloride - 0409-2266-05 - (ALFENTANIL HYDROCHLORIDE)
Drug Information of Alfentanil Hydrochloride
| Product NDC: | 0409-2266 |
| Proprietary Name: | Alfentanil Hydrochloride |
| Non Proprietary Name: | ALFENTANIL HYDROCHLORIDE |
| Active Ingredient(s): | 500 ug/mL & nbsp; ALFENTANIL HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alfentanil Hydrochloride
| Product NDC: | 0409-2266 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075221 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111010 |
Package Information of Alfentanil Hydrochloride
| Package NDC: | 0409-2266-05 |
| Package Description: | 10 AMPULE in 1 CARTON (0409-2266-05) > 5 mL in 1 AMPULE |
NDC Information of Alfentanil Hydrochloride
| NDC Code | 0409-2266-05 |
| Proprietary Name | Alfentanil Hydrochloride |
| Package Description | 10 AMPULE in 1 CARTON (0409-2266-05) > 5 mL in 1 AMPULE |
| Product NDC | 0409-2266 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ALFENTANIL HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111010 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | ALFENTANIL HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
