NDC 0409-2634 – Hydromorphone Hydrochloride
Hydromorphone Hydrochloride 10 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous
Product NDC0409-2634
Product details
- Brand name
- Hydromorphone Hydrochloride
- Generic name
- Hydromorphone Hydrochloride
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intramuscular, Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA078591
- Marketed since
- July 31, 2008
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Hydromorphone Hydrochloride 10 mg/mL
Uses, dosage, side effects and warnings for Hydromorphone Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0409-2634-01 | 10 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-01) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-2634-10) | Aug 8, 2008 |
| 0409-2634-05 | 10 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-05) / 5 mL in 1 VIAL, SINGLE-DOSE (0409-2634-25) | Aug 7, 2008 |
| 0409-2634-50 | 1 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-50) / 50 mL in 1 VIAL, SINGLE-DOSE | Jul 31, 2008 |
Recalls mentioning this NDC
- D-0597-2018 Mar 21, 2018 · Class I
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked. - D-1081-2017 Aug 16, 2017 · Class II
Presence of Particulate Matter: Silicone oil - D-0044-2015 Oct 29, 2014 · Class II
Lack Of Assurance Of Sterility: Confirmed customer complaints of glass product container vials that may be broken or cracked.
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