NDC 0409-1304 – Hydromorphone Hydrochloride
Hydromorphone Hydrochloride 4 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous
Product NDC0409-1304
Product details
- Brand name
- Hydromorphone Hydrochloride
- Generic name
- Hydromorphone Hydrochloride
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Solution
- Route
- Intramuscular, Intravenous, Subcutaneous
- Marketing category
- NDA · NDA200403
- Marketed since
- December 1, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Hydromorphone Hydrochloride 4 mg/mL
Uses, dosage, side effects and warnings for Hydromorphone Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0409-1304-31 | 10 CARTRIDGE in 1 CARTON (0409-1304-31) / 1 mL in 1 CARTRIDGE (0409-1304-03) | Dec 1, 2011 |
Recalls mentioning this NDC
- D-1167-2017 Sep 27, 2017 · Class II
Lack of sterility assurance: resulting from use of a damaged sterilizing filter for nitrogen used in the manufacturing process. - D-020-2013 Oct 31, 2012 · Class I
Superpotent (Single Ingredient) Drug: The prefilled cartridge unit has been found to be overfilled and contain more than the 1 mL labeled fill volume. - D-1444-2012 Aug 15, 2012 · Class I
Superpotent (Single Ingredient) Drug: Some of the prefilled cartridge units have been found to be overfilled and contain more than the 1 mL labeled fill volume.
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