NDC 0703-0018 – Hydromorphone Hydrochloride
Hydromorphone Hydrochloride 10 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous
Product NDC0703-0018
Product details
- Brand name
- Hydromorphone Hydrochloride
- Generic name
- Hydromorphone Hydrochloride
- Labeler
- Teva Parenteral Medicines, Inc.
- Dosage form
- Injection, Solution
- Route
- Intramuscular, Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA078591
- Marketed since
- January 18, 2011
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 0703-0018-01 | 1 VIAL in 1 CARTON (0703-0018-01) / 50 mL in 1 VIAL | Jan 18, 2011 |
Recalls mentioning this NDC
- D-0596-2018 Mar 21, 2018 · Class I
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked. - D-1080-2017 Aug 16, 2017 · Class II
Presence of Particulate Matter: Silicone oil - D-1082-2017 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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