Alfentanil Hydrochloride is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Alfentanil Hydrochloride.
| Product ID | 0409-2266_292181b8-7d59-42cd-af14-119edfddb96c |
| NDC | 0409-2266 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Alfentanil Hydrochloride |
| Generic Name | Alfentanil Hydrochloride |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2006-02-20 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA075221 |
| Labeler Name | Hospira, Inc. |
| Substance Name | ALFENTANIL HYDROCHLORIDE |
| Active Ingredient Strength | 500 ug/mL |
| Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule | CII |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2006-02-20 |
| Marketing End Date | 2021-05-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA075221 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2006-05-04 |
| Marketing End Date | 2019-02-01 |
| Marketing Category | ANDA |
| Application Number | ANDA075221 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-08-30 |
| Marketing End Date | 2016-06-01 |
| Marketing Category | ANDA |
| Application Number | ANDA075221 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-02-20 |
| Marketing End Date | 2011-10-12 |
| Marketing Category | ANDA |
| Application Number | ANDA075221 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2006-02-20 |
| Marketing Category | ANDA |
| Application Number | ANDA075221 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2006-07-13 |
| Marketing End Date | 2015-05-01 |
| Ingredient | Strength |
|---|---|
| ALFENTANIL HYDROCHLORIDE | 500 ug/mL |
| SPL SET ID: | 9781f06d-485e-41f0-84aa-ee177f0ad137 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0409-2266 | Alfentanil Hydrochloride | Alfentanil Hydrochloride |
| 17478-067 | Alfentanil Hydrochloride | Alfentanil Hydrochloride |
| 17478-841 | Alfentanil | Alfentanil Hydrochloride |