NDC 0143-9392 – Remifentanil Hydrochloride
Remifentanil Hydrochloride 2 mg/2mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC0143-9392
Product details
- Brand name
- Remifentanil Hydrochloride
- Generic name
- Remifentanil Hydrochloride
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA210594
- Marketed since
- May 15, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Remifentanil Hydrochloride 2 mg/2mL
Uses, dosage, side effects and warnings for Remifentanil Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0143-9392-10 | 10 VIAL in 1 CARTON (0143-9392-10) / 5 mL in 1 VIAL (0143-9392-01) | May 15, 2021 |
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- 63323-724 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.
- 0143-9393 Remifentanil Hydrochloride 5 mg/5mL · Injection, Powder, Lyophilized, For Solution · Hikma Pharmaceuticals USA Inc.