NDC 63323-724 – Remifentanil Hydrochloride
Remifentanil Hydrochloride 1 mg/mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC63323-724
Product details
- Brand name
- Remifentanil Hydrochloride
- Generic name
- Remifentanil Hydrochloride
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA206223
- Marketed since
- January 19, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Remifentanil Hydrochloride 1 mg/mL
Uses, dosage, side effects and warnings for Remifentanil Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 63323-724-05 | 10 VIAL, SINGLE-DOSE in 1 CARTON (63323-724-05) / 5 mL in 1 VIAL, SINGLE-DOSE (63323-724-01) | Jan 19, 2018 |
Other Remifentanil Hydrochloride products
- 63323-723 Remifentanil Hydrochloride 1 mg/mL · Injection, Powder, Lyophilized, For Solution · Fresenius Kabi USA, LLC
- 63323-725 Remifentanil Hydrochloride 1 mg/mL · Injection, Powder, Lyophilized, For Solution · Fresenius Kabi USA, LLC
- 0143-9391 Remifentanil Hydrochloride 1 mg/mL · Injection, Powder, Lyophilized, For Solution · Hikma Pharmaceuticals USA Inc.
- 0143-9392 Remifentanil Hydrochloride 2 mg/2mL · Injection, Powder, Lyophilized, For Solution · Hikma Pharmaceuticals USA Inc.
- 0143-9393 Remifentanil Hydrochloride 5 mg/5mL · Injection, Powder, Lyophilized, For Solution · Hikma Pharmaceuticals USA Inc.